Open access peer-reviewed chapter

Synthesis, Structure and Biological Activity of Ephedra Heterocycles

By Alejandro Cruz, Itzia I. Padilla‐Martínez and María Esther Bautista‐ Ramírez

Submitted: June 15th 2016Reviewed: January 5th 2017Published: July 12th 2017

DOI: 10.5772/67387

Downloaded: 1400

Abstract

Ephedra compounds are well known due to their biological activity. They have been widely used in asymmetric synthesis during the last decades. Recently, we have prepared reviews about the synthesis of acyclic and heterocyclic ephedra derivative compounds reported in the literature. In this chapter, the synthetic methodology to access acyclic and heterocyclic compounds derived from ephedra alkaloids and its structural analysis are discussed, included those due to the substitution of the hydroxy group by chlorine, sulfur, selenium, or nitrogen atoms. Biological activity analysis of some synthesized compounds was done, and some of them have displayed biological activity.

Keywords

  • ephedrines
  • chirality
  • configuration
  • biological activity
  • stereoespecificity

1. Introduction

Chirality in biological systems is of main significance since in enzymes and drug receptors, the active sites are chiral, and they only interact with molecules of specific configuration. This has synthetic chemists became convinced to accept that all compounds used as pharmaceuticals must be in one of their enantiomeric forms. As a consequence, in the 1980s decade, the Food and Drug Administration (FDA) required pharmaceutical industry to acquire drug candidates in details of the toxic effects of the enantiomers. By this, chemical substances to be used as drugs candidates must be synthetized as optically pure compounds or to be highly enriched.

Biologically active chiral molecules have been extracted from natural products has plants. Extracts from the Ephedrasp. genus have been traditionally used in Chinese medicine as nasal descongestives, cardiac stimulant, and antiasthma agents. The active principle from this plant was first extracted in 1885, isolated, and then purified in 1887 by Nagai [1] who called it ephedrine. The herb, “Ma-Huang” is the best source of ephedrine, up to 1% bulk weight has been obtained from this material. Amounts of pseudoephedrine, N-methylephedrine, N-methylpseudoephedrine, norephedrine, and norpseudoephedrine were found from this herb [2]. Since pharmacologycal studies done by Chen and Schmidt in 1924 [3], the chemists have been interested in the synthesis of physiologically active analogous of ephedrine derivatives [4]. At the present time, large quantities are used in Western medicine to relieve mucous membrane congestion [5].

Today, ephedrine is a pharmaceutical classified as sympathomimetic agent, weaker but longer acting than adrenaline. It acts as cardiac stimulant, hypertensive agent, hyperglycaemic, and bronchodilator. Ephedrine has been clinically used against hay feber, bronchial asthma, myasthenia gravis, whooping cough, Heart block (Stokes-Adam syndrome), and dysmenorrhea. Because ephedrine crosses the hematoencephalic and placentary barriers, have effects on the central nervous system, in consequence, decrease fatigue, sleep (insomnia), and hungry sensations (anorexia) [4].

The no-polar structure of ephedrine makes this substance more liposoluble than catecholamines. It is thermodynamically more stable, in consequence, it is not a substrate for monoamineoxidase (MAO) or the catechol-O-methyltranspherase. Thus, it is a diffusible pharmaceutical that has a more prolonged effect as catecholamines [6].

On the other hand, the modern chemistry is interested in the development of new synthetic methods to produce drugs, antibiotics, alimentary additives, etc., with high optical purity. Asymmetric synthesis design requires catalysts, chiral auxiliaries, and reagents able to control the stereochemistry of the reaction products and to be efficiently recycled [7]. Ephedrines, norephedrines and its derivatives, have been broadly used as chiral auxiliaries in asymmetric synthesis [8]. Thiols, sulfides, and disulfides obtained from ephedrines have been proven to be very good chiral catalysts [9]. It has been found the use of polymer-supported catalysts applied to organic synthesis with emphasis given to the use of ephedrine chiral catalyst to promote asymmetric reactions [10].

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2. Structure of ephedrines

The structure of ephedrine and pseudoephedrine was studied by Ladenburg and Oelschägel. They suggested the formula PhCH(OH)CH(CH3)NHCH3 now accepted for the alkaloids [11]. Studies that support this formula were provided by Schmith and Bümming [12]. The more important fact that ephedrine and pseudoephedrine are stereoisomers is easy with which ephedrine can be isomerized to pseudoephedrine by acylation or by boiling with HCl (25%) [13], this change has been found to be reversible [14, 15].

Freudenberg and Leithe investigated the configuration about C1 and C2 for ephedrine and pseudoephedrine [1618], and represented the distribution about these centers of asymmetry, for ephedrine by structure 1aand for pseudoephedrine by structure 2a, Figure 1.

Figure 1.

Freudenberg and Leithe representation of ephedrine1aand pseudoephedrine2a.

Zhu et al. analyzed the relationship of the substituents of the stereogenic center and to the specific optical rotation. The variables used as matrix elements include (1) the substituent masses (m), (2) radii (r), (3) symmetries (s), and (4) electronegativities (χ) of the atoms or groups bounded to the stereogenic center. For ephedrine and pseudoephedrine, the calculated values were approximate to the observed rotation values [19]. The preferred conformation of ephedrine 1and pseudoephedrine 2was theme of controversy [2025]. The questions could be answered by the X-ray technique.

Several crystal structures of ephedrine salts were reported: the hydrochloride by Bergin [26] and the hydrogen and the di-hydrogen phosphates by Bugg [27, 28] showed the conformation 1b. On the other hand, in an X-ray study, Mathew et al. demonstrated the conformation 2bin structures of (+)-pseudoephedrine and (+)-pseudoephedrine hydrochloride [29]. There was found one strong intermolecular hydrogen bond OH….N in pseudoephedrine which links the molecules into infinite chains around the screw axis. An intramolecular contact N—H---O was observed, but the angle of 108° is not favorable. On the other hand, the C(2)—N bond is nearly parallel to the C(1)—C(ipso) bond. This conformation was also found in a bis-(+)-pseudoephedrine complex of Koper II [30], (−)-noradrenaline [31], and dopamine [32]. Similar conformations for norephedrines were found [33] but the difference in energy levels between the various possible conformations in the nor-series is less than in the ephedrine series, and interconversion is carried out with ease. This was explained because of the hindering effect of the N-methyl group, Figure 2 [34].

Figure 2.

Stable conformations of ephedrine1bandpseudoephedrine2b.

Finally, ephedrines 1,2and norephedrines 3,4have the β-aminoalcohol structure where the phenyl and methyl groups create two chiral centers on each carbon atom and generate four optically active stereoisomers, Figures 4 and 5. Freudenberg et al. [16] and Leithe [17] established the relative configuration about the asymmetric centers for (−)-ephedrine and its optical isomers, hence the configurational relationship between ephedrines 1a,band pseudo-ephedrines 2a,bseries is well known. The stereoisomers with methyl on nitrogen atom are l-(1R,2S)-ephedrine 1aand d-(1S,2R)-ephedrine 1b; d-(1S,2S)-pseudoephedrine 2a,and l-(1R,2R)-pseudoephedrine 2b, Figure 3.

Figure 3.

Ephedrine stereoisomers.

Figure 4.

Norephedrine stereoisomers.

Figure 5.

Some heterocyclic compounds with biological activity.

The l-ephedrine 1ais the stereoisomer that produces a more pronounced stimulus on the central nervous system, compared with other drugs [35].

The stereoisomers without methyl on nitrogen atom are called norephedrines: l-(1R,2S)-norephedrine 3aand d-(1S,2R)-norephedrine 3b; d-(1S,2S) norpseudoephedrine 4a,and l-(1R,2R)-norpseudoephedrines 4b, Figure 4.

3. Physical properties of ephedrines

Physical properties of some optical isomers of ephedrines as free bases or as acidic salts have been summarized, Tables 14 [36].

Characteristicmp (°C)[α]D
Free base (B)37–39−41°
Hemihydrate39–43−6.3° (EtOH)
+11.2° (H2O)
Hydrochloride216–220−34° (H2O)
Hydrobromide205
Sulphete243−30° (H2O)
Oxalate249 (dec)Insol. H2O
Aurichloride128–131
Platinichloride186

Table 1.

(1R, 2S)-(−)-ephedrine forms.

Characteristicmp (°C)[α]D
Free base (B)118–120−51°(EtOH)
Hemihydrate
Hydrochloride185–188−62. (H2O)
Hydrobromide
Sulphete−52.5° (H2O)
Oxalate218 (dec)Insol. H2O
Aurichloride126.5–127.5
Platinilchloride

Table 2.

(1R, 2R)-(−)-pseudoephedrine forms.

Characteristicmp (°C)[α]D (°)
Free base (B)51–54−14.56(EtOH)
Hemihydrate
Hydrochloride172–175−33° (H2O)
Hydrobromide
Sulphete285–286 (dec)−31.99 (H2O)
Oxalate245 (dec)
Aurichloride188
Platinichloride221 (dec.)

Table 3.

(1R, 2S)-(−)- norephedrine forms.

Characteristicmp (°C)[α]D
Free base (B)77–8 (corr.)−37.9 (MeOH)
Hemihydrate
Hydrochloride180–183 (corr.)−41.7° (H2O)
Hydrobromide
Sulphete295 (dec.)−48.7° (H2O)
Oxalate235 (dec.)
Aurichloride137–138
Platinilchloride198

Table 4.

(1R, 2R)-(−)- norpseudoephedrine forms.

4. Biological activity of ephedra heterocycles

A wide approach for the synthesis of new compounds that possess some kind of biological activity is the cyclization of substituted phenethylamines as ephedrines into heterocycles, such as morpholine (phenmetrazine) [37] and 2-amine-oxazolines (4-methylaminorex and 3,4-dimethylaminorex) [38], in such a way that the ephedrine skeleton becomes part of the heterocyclic ring, Figure 5.

Some other heterocycles as oxazolidine [39], di- and tetrahidro-1,3,4-oxadiazines [40, 41], 2-thiazoline [42], thiazolidine [43], dihidro-1,3,4-thiadiazine [44], tetrahydrotriazine [45], and imidazolidine [46] derived from ephedrines and norephedrines have been reported. Certain of these heterocycles exhibit different biological effects as central nervous system, stimulating, appetite-depressing [37, 38], monoamine oxidase inhibiting antidepressant [40g, 44b], central nervous system depressant [40e, f, 41, 45], analgetic [45], hypocholesterolemic [41], anti-inflammatory [41], antimicrobial [41, 44b], or catechol-amine-potentiating [43] activities. On the other hand, 3,4-dimethyl-5-phenyl-oxazolidine is used as a prodrug [47].

5. Reactions to get chlorodeoxyephedrine derivatives

The bromination reaction of ephedrine hydrochloride 2awith PBr5 produce the bromodeoxy-derivative [48]. On the other hand, ephedrine 1aor norephedrine 3aor its hydrochlorides reacts with SOCl2 to give chlorodeoxypseudoephedrine 5aor chlorodeoxynorpseudoephedrine 5b. The same reaction with pseudoephedrines 2aor 4agive a 60:40 diastereomeric mixture of threo:erytho5a:6a, Scheme 1 [49]. In order to improve the stereoselectivity, chlorination reaction of pseudoephedrine stereoisomers 2at 0°C was carried out. In these conditions, only the corresponding threochlorodeoxystereoisomers 3were stereoselectively obtained (SNi mechanism), Scheme 1, the X-ray diffraction structure of 5ais depicted in Figure 6.

Scheme 1.

Chlorodeoxyephedrine hydrochlorides from chlorination reaction of ephedrines2.

Figure 6.

X-ray diffraction structure of Chlorodeoxyephedrine hydrochloride5a.

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6. Heterazolidines-2-heterounsaturated from ephedrines

In 1950, Close reported the solvent-free dehydration of ephedrine hydrochloride 1in the presence of urea at 180–200°C to afford the imidazolidinone 11a-(t) and oxazolidinone 15a-(c), Scheme 2 [34]. In that work, it was proposed that urea is converted into ammonium oxocyanate at 180–200°C, which in the presence of hydrogen chloride, ammonium chloride and oxocyanic acid are produced. Finally, ephedrine reacts with oxocyanide acid to produce the nonisolated urea intermediate 7a-(e), which cyclization by dehydration affords the trans-imidazolidone 11a-(t). On the other hand, in a simultaneous manner, cyclization of urea 7a-(e) by nucleophylic attack of the oxygen atom of ephedrine to the ureidic carbonyl and ammonia elimination produces the oxazolidone heterocycle 15a-(c).

Scheme 2.

Dehydration of ephedrine 1a-(e) with urea according to Close.

The same reaction was revisited with the use of K+NCO instead of urea, and the study was extended with thiocyanates and pseudoephedrine 2a-(th), norephedrine 3b-(e), and norpseudoephedrine 4b-(th), as stereoisomers to produce a series of optically active 1,3-heteroazolidine-2-heterounsaturated compounds 915, Scheme 3.

Scheme 3.

1,3-heterazolidines-2-heterounsaturated from ephedrines.

6.1. Reaction of ephedrines with oxocyanate

Urea intermediate 7a-(e), proposed in the Close’s reaction, was isolated when K+NCO is reacted with ephedrine hydrochloride 1in refluxing ethanol for 72 h (78% yield). The reaction was also performed with pseudoephedrine 2, norephedrine 3,and norpseudoephedrine to afford, the urea derivatives 7a-(th), 7b-(e), and 7b-(th) in 83, 80, and 86% yield, respectively (Scheme 4). In the case of the reaction of Na+NCS with ephedrine stereoisomers series 1–4, only chloride by thiocyanate anion was exchanged to give the corresponding hydrothiocyanates 8a,b(e,th) (Scheme 4). The urea intermediate 7a-(e) derived from ephedrine could be crystallized from ethanol and its structure studied by X-ray diffraction (Figure 7).

Scheme 4.

Reaction of K+NCO and NH4+NCS with ephedrines 1a,b-(e,th) in refluxing ethanol.

Figure 7.

Molecular structure of ephedrine-urea7a-(e).

An intramolecular hydrogen bonding interaction between the hydrogen atom of the hydroxyl group and the ureidic oxygen atom to form a seven membered ring was observed. The O1H1···O6 distance of 1.820(24) Å [angle of 166.72° (2.25)] represents a strong interaction [50]. The formed hydrogen bond forces the NH2 group to adopt a syn conformation to the N-Me group [C8N4C5N7 angle of −6.00 (0.26)°]. In addition, both N—CO bond distances are of intermediate value between a single (1.469 Å) and a double (1.279) N—C bond (1.35 Å mean) [51].

When the intermediate 7a-(e) was free of solvent heated at 180–200°C for 1 hour, an equimolar mixture of imidazolidone 11a-(c) and oxazolidone 15a-(c) was formed (Scheme 5). Imidazolidinone 11a-(c) was separated by precipitation from a CHCl3 and purified by recrystallization from ethanol. The structure of cis(c) isomer instead of the expected trans(t) isomer [52] was observed on the 1H and 13C NMR spectra and confirmed by X-ray diffraction analysis. The formation of an aziridinim isocyanate Ithen the isocyanate IIas intermediates are proposed to explain the retention of C1 configuration in the formation of the cis-imidazolidone 11a-(c) (Scheme 5) [53]. On the other hand, the oxazolidone 15a-(c) is formed in accord to the Close’s idea (Scheme 2). The in situformation of amides from aminoalcohols involved in oxazolidine formation has been reported in the literature [34, 54].

Scheme 5.

Mechanistic pat way for the cyclization of ephedrine-urea7a-(e) to get imidazolidinone11a-(t).

On the basis of these previous findings, the free of solvent reaction of ephedrines 1,4with sodium or ammonium thiocyanates were performed.

6.2. Reaction of ephedrines with thiocyanate

In the direct heating of one equimolar of Na+NCS with ephedrine 1 at 180–200°C during 0.5 h, ephedrine hydrothiocyanate 8a-(e) from the aqueous phase and trans-thiazolidine-2-imino hydrothiocyanate 9a-(t) from the chloroform phase (10% yield) were separated, after CHCl3/H2O partition, Scheme 6. Deamination of ephedrine hydrothiocyanate 8a-(e) proceeded to give Ethylphenylketone as lateral product.

Scheme 6.

Heating reaction of ephedrine1with NaSCN.

The reaction with two molar equivalents of NH4SCN for 4 hours afforded the thiazolidine-2-imino hydrothiocyanate 9a-(t) in 50% yield as precipitate from CHCl3. The use of NH4SCN instead of NaSCN salt, avoided deamination, due to its lower melting point (153°C). Compound 9a-(t) was identified on comparing the structure obtained from chlorodeoxypseudoephedrine [55]. On the other hand, several heterocycles were separated when the remaining chloroform mixture was eluted in a chromatographic column. The mass spectrometry of the separated fractions showed the presence of heterocycles summarized in Table 5.

Heterocycle9101112131415
EphedrineXSNHNHSSOO
YNH2SCNSOSOSO
1a-(e)Cis184 (2)163 (3)
[190(27)]
196 (7)
[223 (100)]
172 (4)160 (2)
[191 (19)]
Trans168(50)
[206(98)]
183 (7)162 (7)195 (2)
[223 (100)]
171(7)191 (23)
1a-(th)Cis169(15)
[206(15)]
184 (40)
[206 (100)]
163 (5)
[190(27)]
196 (6)
[223 (100)]
172
[207(64)]
160 (5)
[191 (19)]
Trans162 (2)Traces
[223 (100)]
171
[207(41)]
159 (20)
[191 (23)]
1b-(e)CisTraces
[192 (100)]
200 (5)
[209 (100)]
176 (5)
[193(16)]
189 (2)
[193 (35)]
160 (40)
[177 (8)]
TransTraces199 (2)
[209 (100)]
175(40)
[193(25)]
1b-(th)Cis173(40)
[192(62)]
183 (10)
[192 (100)]
200 (15)
[209 (100)]
175(10)
[193(16)]
160 (3)
Tans172(10)174 (5)159 (3)

Table 5.

Carbonyl carbon chemical shift in ppm, proportion (%) and mass spectrometry data [M+ (%)] of heterocycles 9–15.

As described above for ephedrine 1, two molar equivalents of NH4+NCS were heated with pseudoephedrine 2, norephedrine 3, and norpseudoephedrine 4. The identified compounds are listed in Table 5.

The reaction mixture of pseudoephedrine hydrochloride 2was treated with a 50:50 of CHCl3/H2O mixture. The chloroform phase was eluted in a column chromatography. Using chloroform as eluent, the imidazolidine-2-thione 10a-(c) was separated in 40% yield as first fraction. Imidazolidones 11a-(c) and 11a-(t), thiazolidinedione 12a-(c), and thiazolidinones 13a-(c) and 13a-(t) were separated in small quantities in the subsequent three remaining fractions, respectively. On the other hand, after evaporation of the aqueous phase, thiazolidine-2-imino hydrothiocyanate 9a-(c) and oxazolidinones 15a-(c) and 15a-(t) as solid mixtures were identified by mass spectrometry. NMR spectral data of compound 10a-(c) show a broad signal at 6.32 ppm (1H) and at 183 ppm (13C) of the N—H and C—S groups, respectively. The molecular ion [z/e = 206 (100%), M+] and X-ray diffraction analysis confirmed the structure, Figure 8. The bond distances C2—N1 [1.345(14) Å] and C2—N3 [1.332(13) Å] show an intermediate value between a single and a double bond [51], due to a conjugation through the N1—C2—N3 fragment.

Figure 8.

Structure of imidazolidinethione10a-(c).

From the reaction mixture of norephedrine hydrochloride 3, compounds 13b-(c) and 13b-(t) in a 1:8 proportion were separated by chromatography. Compound 13b-(t) (40% yield) was separated from 13b-(c) in a second column using CHCl3. The spectra data, molecular ion [z/e = 193 (25%), M+], and the X-ray diffraction structures of compound 13b-(t) confirm the transconfiguration (Figure 9). A conjugation through the N—C2—S fragment is observed because the bond distances C2-N [1.332(3) Å] and C2-S [1.775(2) Å] are shorter than the corresponding single bonds.

Figure 9.

Structure oftrans-thiazolidinone13b-(t).

The reaction mixture of norpseudoephedrine hydrochloride 4was separated in a chromatographic column and each fraction analyzed by mass spectrometry, Table 5. The fourth fraction contained thiazoline-2-amine hydrothiocyanate 9b-(c).

At least four competitive mechanisms are proposed to explain the formation of heterocycles 9-15a,bin the heating reaction of NH4SCN with ephedrines 1,2and norephedrines 3,4(Scheme 7). In general, with exception of heating reaction of norephedrine 3, a SN2 dehydration mechanism by the thiocyanate = isothiocyanate anions as nucleophiles and the subsequent cyclization of the ephedrinethiocyanate (IV) and/or ephedrineisothiocyanate (III) intermediates formed operate to give the corresponding thiazolidine-2-imino hydrothiocyanates 9a,band/ or imidazolidinetiones 10a,b. The product from thiocyanate predominate in the heating reaction of ephedrine 1, and for pseudoephedrine 2, the product from isothiocyanate predominate. A stable alkyl ephedrinethiocynate analogue to IVhas been isolated, which support the proposed mechanism [56].

Scheme 7.

Proposed mechanisms to explain the formation of heterocycles915.

In the heating reaction of norephedrine 3, the H2S obtained by hydrolysis of thiocyanate acts as nucleophyle in competitive SN1 and SN2 mechanisms to form the thiolephedrine thiourea VI-(e,th), which cyclization afford thiazolidinethiones 12b(c,t). A desulphurization by hydrolysis of thiazolidinethiones 12b-(c,t) explains the formation of thiazolidinones 13b-(c,t). A mechanism through thioureidic intermediate Voperates simultaneously, its cyclization affords oxazolidinethione 14b-(c), which desulphurization gives oxazolidinone 15b-(c).

Desulphurization of the oxazolidinethione 14a-(t) explains the formation of oxazolidinone 15a-(t) (20%) in the heating reaction of pseudoephedrine 2, Scheme 6, this mechanism is favored when one molar equivalent of NH4+NCS is used. In this case, oxazolidinone 15a-(t) (40%) and imidazolidinethione 10a-(c) (20%) were obtained as the major products. Similar results were observed in the heating reaction of norpseudoephedrine 4. If NH4+NCS is changed from two to one molar equivalents, thiazoline-2-amine hydrothiocyanates 9b-(c) decreased from 40 to 15% and oxazolidinone 15b-(t) increased from 3 to 45%.

In general, in the 1H NMR spectral data of ephedracycles, the C—CH3 group of the cisisomers appears at low frequency shifts in the range between 0.9 and 0.7 ppm, compared with the same group of the transisomers, appearing between 1.1 and 1.4 ppm, this is due to the shielding effect of the phenyl group.

7. Heterazolidines-2-heteroinsaturated from chloropseudoephedrines

In continuation with our investigations on the design of new heterocycles derived from ephedrines 1, in this work, we revisited the cyclization reactions of chlorodeoxypseudoephedrine hydrochloride 5a-(th) (R = Me) with one or two molar equivalents of potassium oxocyanate, sodium thiocyanate, and potassium selenocyanate nucleophiles as cyclizing agents in refluxing ethanol. In addition, the results of the reaction of chlorodeoxynorpseudoephedrine hydrochloride 5b-(th) (R = H) with the above mentioned nucleophiles are reported. An interesting finding of this study was the synthesis of the transisomer of 1,3-oxazolidine-2-iminium chloride 18a-(t) through the in situchlorinated urea intermediate 7a-(e), Scheme 8.

Scheme 8.

Reactivity of chlorodeoxypseudoephedrine hydrochlorides5with heterocyanates.

7.1. Reaction of chlorodeoxypseudoephedrine hydrochlorides 5 with potassium oxocyanate

Chlorodeoxypseudoephedrine hydrochloride 5a-(th) was reacted with two molar equivalents of KOCN in stirring ethanol at room temperature. The reaction was monitored at 24, 48, and 72 h by 1H NMR. Two compounds, in 80:20, 60:40, and 40:60 proportions, respectively, were observed. The NMR tube of the 40:60 proportion in DMSO-d6 was heated at 92°C during 1 h, to quantitatively transform the minor proportion compound into the 1,3-oxazolidine-2-iminium oxocyanate 18a-(c) identified as the only product. The N-(1-chloro-1-phenyl-2-methyl-ethyl)-N-methyl urea 17a-(th) in the 80:20 mixture with 18a-(c) was identified as the intermediate. The use of one molar equivalent of potassium oxocyanate in the same reaction in refluxing 16 h afforded the hydrochloride of the oxazolidine-2-imine 18a-(c), which was crystallized from ethanol to be analyzed by X-ray diffraction, the structure is shown in the Figure 10.

Figure 10.

Molecular structure of hydrochloride compound18a-(c).

The reaction is general; the reaction of one molar equivalent of KOCN with chlorodeoxynorpseudoephedrine hydrochloride 5b-(th) (R = H) in refluxing ethanol 8 h afforded the chlorourea derivative 17b-(th). The proposed mechanistic pathway represented in Scheme 9 explains why the reaction is carried out with inversion of the Cl configuration to get the cisisomer.

Scheme 9.

Mechanistic pathway involved in the synthesis of compounds18a-(c) and18b-(c).

Chlorourea compound 17b-(th) could be isolated and characterized by NMR. Two signals are observed in the 1H NMR spectrum 6.04, (d, 3J= 8.5 Hz) and 5.55 ppm (s, broad) in a 1:2 proportion, respectively, assigned to NH and NH2 urea hydrogen atoms, respectively. The NH coupling constant value proposes a hydrogen bonding NH---Cl interaction, which makes this hydrogen and H2 to be in an antiposition. In addition, the small H1, H2 coupling constant (3J = 5.28 Hz) supports this proposed interaction, Figure 11. The 13C NMR spectrum shows the carbonyl carbon signal at 159.6 ppm, according to the proposed structure.

Figure 11.

Hydrogen bonding interaction proposed in compound17b-(th).

The chlorourea derivative 17b-(th) was refluxed in ethanol during 24 h. The 1H NMR spectrum of the solid precipitated showed a 80:20 mixture of two heterocycles. The 1H NMR chemical shift of the +NH3 group appears in 9.65 ppm as a broad signal, H5 and H4 appear at 6.49 (d) and 4.56 ppm (dq), for the major compound. For the minor compound, H5 and H4 appear at 5.26 (d) and 5.41ppm (dq), respectively. In both compounds, the coupling constants are of the same value. In addition, the multiplicity of these signals are interchanged for the minor compound, which are correlated with 13C NMR signals at 65.9 (C4) and 84.6 (C5) ppm, respectively. These results allowed us to assign the cis-4-methyl-5-phenyloxazoline-2-ammonium chloride 18b-(c) as the major compound the cis-5-methyl-4-phenyl-oxazoline-2-ammonium hydrochloride 23b-(c), as the minor compound, whose formation is explained due to the participation of an aziridine intermediate III, Scheme 10 [52].

Scheme 10.

Mechanistic pathway proposed to explain the formation of compound23b-(c).

It is known that in chlorination reaction of ephedrine derivatives with thionyl chloride, the C1 configuration is retained through a SNi mechanism, when ephedrine bears a bulky group as oxamide or sulfonamide on the nitrogen atom [57]. In this sense, we obtained the erythroisomer of ephedrineurea intermediate 7a-(e) by the reaction of ephedrine hydrochloride 1a-(e) with KOCN [58]. This ephedrineurea was chlorinated with thionyl chloride in CHCl3 to get, in situ, 1-(2-chloro-1-methyl-2-phenyl-ethyl)-1-methyl-urea 17a-(e). Compound 17a-(e) was refluxed in ethanol during 8 h. 1H and 13C NMR spectroscopic data of the solid obtained after solvent removal allowed us to identify the transisomer of 3,4-dimethyl-5-phenyl-oxazolidine-2-iminium chloride 18a-(t). This result showed that chlorodeoxyephedrine urea 17a-(e) was obtained with retention of C1 configuration, which was cyclized with the inversion of C1 configuration to obtain 18a-(t). In a similar manner, the same reaction with norephedrine hydrochloride 1b-(e) is stereoselective to get the cisisomer of the oxazoline-2-ammonium chloride 18b-(c). In contrast, the same procedure for pseudoephedrine 1a-(th) and norpseudoephedrine 1b-(th) hydrochlorides gave a mixture of oxazolidine-2-iminium chlorides 18a(60:40, c:t) and oxazoline-2-ammonium chlorides 18b(75:25, c:t), respectively [59].

7.2. Reaction of chlorodeoxypseudoephedrine hydrochlorides 2 with sodium thiocyanate

It is known that the condensation reaction of chlorodeoxypseudoephedrine hydrochloride 5a-(th) with two molar equivalents of NaSCN in refluxing ethanol for 8 h stereoselectively affords the trans-thiazolidine-2-iminio thiocyanate 9a-(t) [51].

The reaction of chlorodeoxynorpseudoephedrine hydrochloride 5b-(th) (R = H) with two molar equivalents of KSCN in refluxing ethanol, only chloride is interchanged by thiocyanate anion to give chlorodeoxynorpseudoephedrine hydrothiocyanate 16b-(th) (ν= 2057 cm−1, SCN), even at 24 h of reflux. If hydrothiocyanate 16b-(th) in DMSO-d6 is heated (90°C) 1 h in a NMR tube, a 50:50 cis/transmixture of 1,3-thiazoline-2-ammonium thiocyanate 9bwas detected in the 1H NMR spectrum. However, only the cisisomer of 9b-(c) was stereoselectively produced if the reaction is solvent free heated at 170°C during 3 hours, Scheme 8.

7.3. Reaction of chlorodeoxypseudoephedrine hydrochlorides 2 with potassium selenocyanate

As previous result reported for chlorodeoxypseudoephedrine hydrochloride 5a-(th) [51], the reaction of chlorodeoxynorpseudoephedrine hydrochloride 5b-(th) with two equivalents of KSeCN in refluxing ethanol for 10 hours affords trans-selenazoline-2-ammonium selenocyanate 19b-(t). On the other hand, if only one equivalent of KOCN, NaSCN, or KSeCN is used in the reactions, the corresponding hydrochloride salts of the 2-aminoheterocyles are obtained. Both XCN (X = O, S, Se) and Cl salts were liberated with aqueous NaOH to give the corresponding imine 20–22aor amine 20–22bcompounds. Compound 20b-(c) and 22b-(t) were crystallized from ethanol and chloroform, respectively. The structures could be established for X-ray diffraction analysis, Figures 12 and 13, respectively.

Figure 12.

X-ray diffraction structure of20b-(c).

Figure 13.

X-ray diffraction structure of22b-(t).

8. CIS-thiazolidinethiones from chloropseudoephedrines

In 1995, we reported the reaction of chlorodeoxypseudoephedrine.hydrochloride 5a-(th) with 33% aqueous solution of sodium trithiocarbonate (Na2CS3) in refluxing ethanol to give cis-thiazolidinethione 12a-(c) (53% yield), Scheme 11 [60]. However, the same reaction with chlorodeoxynorpseudoephedrine 5b-(th) failed to give the corresponding cis-thiazolidinethione derivative 12b-(c).

Scheme 11.

Mechanistic transformation to getcis-thiazolidinethiones from chlorodeoxypseudoephedrines.

By this, we encourage us the goal to selectively obtain cis- or trans-thiazolidinethiones 12a,bfrom either chlorodeoxynorpseudoephedrine 5bor chlorodeoxypseudoephedrine 5aderived from ephedrines 1,3.

To get thiazolidinethiones 12a,b, the chlorhydrates of chlorodeoxypseudoephedrines 5aor 5bwere reacted with one molar equivalent of sodium dithiocarbonate in ethanol solution at room temperature. In the case of chlorodeoxynorpseudoephedrine·HCl 5b, a white powder solid was precipitated in stirring ethanol for 6 h. The cisand transrelationships between the phenyl and the methyl groups in thiazolidinethiones 12bwas deduced from the analysis of their 1H and 13C NMR spectral data and are in agreement with data reported [49d]. On this bases, the product represented a mixture of cis:trans-thiazolidinethiones of 8in a 9:1 proportion. A SN2 mechanism to explain the C1 inversion of configuration, then cyclization to get the cis-isomer is proposed to be carried out, Scheme 11. In addition, a competitive double SN2 mechanism on C1, then cyclization in which cis-aziridine 24b-(c) as intermediate is involved to explain the presence of the trans-isomer 12b-(t). Analogous mechanistic observations were proposed to get stereospecifically thiazolidinethiones from the reaction of viciodoalkanecarbamates with potassium ethylxanthate [61]. When the same reaction at 0°C for 6 h was performed, only cis-thiazolidinethione 12b-(c) was precipitated as a white powder in 95% yield. Thiazolidine-thione 12b-(c) is stable as thione tautomer in concentrated solution (δNH at 8.3 ppm). However, in a diluted solution, the thiol tautomer is present (δSH at 1.6 ppm).

The reaction of chlorodeoxypseudoephedrine·HCl 5aat 0°C was performed, and after 3 days off, white orthorhombic crystals of cis-thiazolidinethione 12a-(c) precipitated in 81% yield. The X-ray diffraction structure showed the cis-isomer.

To confirm that the cis-aziridine is responsible of the trans-thiazolidinethione formation, the Kelloggs method was used with the previously obtained cis-aziridine 24a-(c) and 24b-(c) [62] from chlorodeoxypseudoephedrines 5aor 5b. The corresponding cis-aziridine was reacted with CS2 in stirring ethanol by 48 h at 0°C. In the case of the reaction of cis-aziridine 24b-(c), two compounds in a 70:30 mixture were observed in the 1H NMR spectra. The CH3 groups of the two compounds were in 1.35 and 1.44 ppm, respectively. After comparison with reported data, both compounds were identified as transisomers of thiazolidinethiones [63]. The major heterocycle was the trans-thiazolidine-thione 12b-(t) and the minor heterocycle, the trans-isothiazolidinethione 25b-(t). The ring opening on C3 and C2 of the aziridinium by the aziridinethiocarbamate anion of the intermediate IIIexplains the formation of both heterocycles, Scheme 12. This aziridinium opening reaction has been observed elsewere [59, 62].

Scheme 12.

Mechanistic transformation ofcis-aziridine4cinto a mixture oftrans-thiazolidinethione8tandtrans-isothiazolidinethione10t.

When cis-aziridine 24a-(c) was reacted with CS2, in the same reaction conditions, cis-thiazolidinethione 12a-(c) was stereoselectively obtained instead of the expected trans-isomer in agreement with the Kellog’s method, Scheme 13. In this case, the retention of the C1 configuration is explained by attack of the aziridinium thiocarbamate zwitterion VIon the benzylic carbon, followed by the closure of the intermediate VIIto recover the initial C1 configuration.

Scheme 13.

Mechanistic transformation ofcis-aziridine24a-(c) intocis-thiazolidinethione12a-(c).

Crystals of Cis-thiazolidinethione 12a-(c) were separated from ethanol and its structure studied by X-ray diffraction analysis, Figure 14. The N3—C2(S2)—S1 conjugated system is proposed since the distances are of an intermediate value between a single (1.469 Å) and a double (1.279 Å) N—C bond (N3—C2 = 1.35 Å) and a single (1.789 Å) and a double (1.600 Å) C—S bond (S1—C2 = 1.741Å and S2—C2 = 1.659) [51]. Conjugation makes N3 to be in a sp2 hybridation, as the angles C(4)—N(3)—C(12) = 119.9(3), C(2)—N(3)—C(4) = 116.2(3), and C(2)—N(3)—C(12) = 121.6(3) show values close to 120°. On the other hand, the five membered ring is almost planar since the torsion angles N(3)—C(2)—S(1)—C(5) of 5.3(3)°, S(2)—C(2)—N(3)—C(12) of −1.8(5)° are very close to 0°, and S(2)—C(2)—S(1)—C(5) of −177.4(2)°, S(1)—C(2)—N(3)—C(12) of 175.1(3) are close to 180°. An intramolecular contact between a hydrogen atom of the N—CH3 group and the sulfur atom of the thiocarbonyl group occurred to form a five member ring. The C12H12S2 distance of 2.72(4) Å [angle of 111(3)°] is in the range for a strong interaction [50].

Figure 14.

X-ray diffraction structure ofcis-tiazolidinethione12a-(c).

9. Thiazaborolidines from thioephedrines

The synthesis of N-alkyloxazaborolidines 2628derived from ephedrines has been reported (Figure 15) [64]. In 1995, we reported the analogous compounds made from thioephedrines, and herein, we report several borohydrides derived from thioephedrine (compounds 12a, 29–37) following the syntheses depicted in Scheme 14.

Figure 15.

Borolidines from ephedrines.

Scheme 14.

Thiazaborolidines from ephedrines.

Hydrolysis of thiosulfate 29obtained with retention of C1configuration from the substitution reaction of chloride 5give the disulfide 30, Scheme 14. The disulfide 30reacts with BH3-THF to give a mixture of the stable N-epimers disulfide amine boranes 31and 32detected by 11B NMR. This N-epimers are comparable with the N-BH3 adducts of pseudo-ephedrines.

Heating the N-epimers mixture of 31+ 32, affords the borinic ester 33as the only product, which in the 11B NMR spectra appears as a triplet [(δ= −6.4 ppm, J(BH) = 103 Hz, in CDCI3 or δ= −4.5 ppm, in THF-d8]. Two methyl groups in transposition was found for borinic ester 33on the 1H and 13C NMR data. This allows us to assign the configuration at the nitrogen atom. No borinic esters with a BH2 group derived from ethanolamines as stable compounds have been observed. Borinic ester 33was distilled in vacuo, and on the 11B NMR spectra of the distillated, a mixture of thiazaborolidine 33, 10%, and thiazaboroline 34were observed. Slowly elimination of H2 transforms borinic ester 33into thiazaboroline 34. In the 11B NMR spectrum, compound 34shows a doublet (δ= +40.8 ppm, J(BH) = 154 Hz). From the distilled, a crystal of compound 33was separated and its X-ray diffraction structure obtained (Figure 16). The thiazaboroline 34reacted with BH3-THF to afford the N—BH3 adduct 35(Scheme 1). The structure has been deduced from the 11B NMR data, which indicated a N—BH3 bond (quadruplet at δ= −22.0 ppm, J(BH)= 71 Hz) and a doublet which is strongly shifted to lower frequencies (δ= −7.0, J(BH)= 148 Hz). A diborane group in which a hydrogen atom from the N—BH3 adduct is bridging the boron atom of the heterocycle was found. These findings are similar to that found in the pseudoephedrine oxazaborolidine [64a].

Figure 16.

X-ray diffraction structure of borolidine33.

Thiazolidine-2-thione 12a-(c) obtained from compound 5awith sodium trithiocarbonate has been isolated and its reactivity towards BH3-THF studied, Scheme 14. The reaction was followed by 11B NMR, and a S—BH3 adduct 36(δ= −23 ppm, broad signal) was first detected. The analysis of 1H NMR spectrum of compound 36indicates that BH3 is linked to the thione sulfur atom. Heating the S—BH3 adduct 36afforded the thiazaborolidine 37which is a triplet at δ= −3.8 ppm (J(BH) = I I 1.5 Hz) in 11B NMR spectra. This compound 37is obtained pure when 12a-(c) is reacted with 3 equivalents of BH3-THF. The 1H and 13C NMR were recorded. The diasterotopic N-methyl groups show that the nitrogen has a stable configuration, the assignment of the 1H and 13C signals was done by comparison with similar compounds [64b, 65].

Compound 33has the C-5 atom out of the plane of an envelope conformation of the five member ring. The N—B bond distance is 1.58(1) Å and B—S of 1.922(9) Å. Boron and nitrogen atoms are tetrahedral. The nitrogen atom was found to be of “S” configuration, as deduced from the 1H and 13C NMR data. The methyl groups are transposition. The angles on the nitrogen atom are close to a sp3 hybridation, C4—N3—C13 112.3(5)°, B2—N3—C13 111.3(5)°, and C4—N3—B2 112.0(5)°.

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10. Biological properties of ephedrines and their derivatives

10.1. Ephedrines

Mao (Ephedra sinica Stapf), which provides similar effects to ephedrine [66, 67], is used as a component of several herbal medicines. It has been utilized in the treatment of cold and allergy [68, 69]. Clinically, it is utilized to lower fever, relieve pain and headaches, control body weight, relieve inflammatory responses [70, 71], and also rheumatoid arthritis [72].

Ephedrine 1aand pseudoephedrine 2aare also used to treat cancerous diseases in modern clinical practice, they combined with other preparations relieve arterial spasms, neurotoxic reactions after radiation therapy and chemotherapy [73, 74].

Since 1938, ephedrine was regulated as a drug; however, the herbal source was regulated as a food. However, after the Dietary Supplement Health and Education Act of 1994 (DSHEA) [75] was passed, the herbal products escaped drug regulation. As a consequence, ephedra extracts remains available as a “dietary supplement.” However, after years of battling, stimulant combination products (e.g., ephedra and caffeine) are yet available.

10.2. Chloroephedrine derivatives

Previously was demonstrated that N-β-chloroalkylamine derivatives 5a,b(Figure 17) possess a different spectrum of anticancer activities [76]. On the other hand, cytotoxic and antitumor activities of ephedrine and N-β-chloroalkylamine derivatives 5a(13), 5b(13) were determined [77].

Figure 17.

Structures of N-β-chloroalkylamine derivatives5a,b.

It was found compounds 5b1, 5b2, and 5b3were active in the cytotoxicity test for 3H-thymidine incorporation. The concentrations causing 50% cytotoxicity were in the range 11.0–45.0 mg/mL. However, derivatives 5a1, 5a2, and 5a3were more active.

Compounds 5a2, 5b2, 5a3, and 5b3investigated in vitrosuppressed growth of EAC and S-180 tumor strains to various degrees.

It has been shown that the introduction of phosphorus-and sulfur-containing fragments considerably lowers the toxicity of the alkaloids.

With respect to substances 5a1and 5b1, they had similar toxicity to l-ephedrine, while the other substances were less toxic. It has been found that the replacement of the oxygen atom in the structure of a thio salt of/l-ephedrine 5a3by a second sulfur atom led to a slight rise in toxicity.

10.3. Dithiocarbamate derivatives

N-methyl-l-ephedrinedithiocarbamates derived from l-ephedrine 1aand d-pseudoephedrine 2ahas been obtained. Dithiocarbamic acid derivatives exhibit a broad-spectrum physiological activity [78]. They were found to act as fungicides, herbicides, insecticides, acaricides, zoocides, nematocides, growth regulators, bactericides, etc. Such dithiocarbamic acid derivatives as Carbathion, Cineb, Vegadex, and Cyram have found practical application in agriculture as pesticides.

10.4. Oxazolidines derivatives

Due to the reversibility of the reaction of ephedrines 14with aldehydes or ketones to get oxazolidine heterocycles (Scheme 15), these compounds could be used as prodrugs [79]. Some of these compounds significantly increased locomotor activity in rats at 50-mg/kg dose. The formaldehyde derivative had similar activity as ephedrine. All other compounds were less active.

Scheme 15.

Oxazolidines from ephedrine.

Four such compounds were tested in rats for ephedrine-like activity using the hyperthermia and anorexia models. The results showed that all of the compounds decreased food intake significantly, but only the acetone and the salicylaldehyde derivatives caused a significant elevation of body temperature [80].

On this bases, we probed the antioxidant and antimicrobial activity of some heterocyclic compounds derived from ephedrines 14previously synthetized.

11. Determination of biological activity of ephedracycles

Ephedrine is a very good pharmaceutical but it acts as central nervous system stimulant, and ephedrine and their derivatives have been used as drugs of abuse so its prescription has been restricted, we proposed ephedra heterocycles as new derived compounds as pharmaceutical candidates with low central nervous system. We decided to prove the antioxidant and antibiotic activities of several heterocycles synthetized in our laboratory represented in Tables 6 and 7, respectively.

Table 6.

Antioxidant activity (IC50 mol/L) of some synthetized heterocyclic compounds.

CompuestoSalmonella typhiStaphylococcus aureusEscherichia coliBacillus subtilis
21bNANANANA
342081020
9tNANANANA
21aNA6NA9
19tNANANANA
22aNANANANA
12tNANANANA
12acNANANANA

Table 7.

Antibiotic activity of some synthetized heterocyclic compounds derived from ephedrine 1–8.

Inhibition in mm.


No actividad found (NA).


11.1. Antioxidant activity

The DPPH radical scavenging activity of plants was estimated according to the method explained by Cheung, with some modifications. Aliquots of 2 ml of 6 × 10−5 M DPPH methanol were mixed with 50 μL of the extracts. The mixtures were vigorously shaken and left to stand for 10 min under subdued light. The absorbance at 540 nm was measured against methanol as a blank. The decolorization was spectrophotometrically measured at 517 nm. The radical scavenging activity (RSA) was calculated using the equation:

%RSA=100×(1AE/AD)E1

AEis the absorbance of the solution containing antioxidant extract, whereas AD is the absorbance of the DPPH* solution.

Compounds 34, 19t, and 12tshowed antioxidant activity, Table 6.

11.2. Antimicrobial activity

Disk diffusion assay: extracts were tested for antibiotic activity against Escherichia coli, Salmonella thypi, Staphylococcus aureus, Bacillus subtilis, and Candida albicans. About 50 μL of extract was solubilized in ETOH and placed on the surface of the inoculated agar and incubated at 30°C, using antibiotic no. 1 medium, and the antibiotic activity was recorded as the diameter of clear zones of inhibited microbial growth around the paper disk.

The antimicrobial activity was determined using strains S. aureus, B. subtilis, S. thypi, and E. coliusing sensidiscs. The antioxidant activity was measured by the radical 2-2-diphenyl-1-picrihydrazil. Compound 34presented antimicrobial activity against all microorganisms used and the compound 21ashowed activity only against S. aureusand B. subtilis, Table 7.

© 2017 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Alejandro Cruz, Itzia I. Padilla‐Martínez and María Esther Bautista‐ Ramírez (July 12th 2017). Synthesis, Structure and Biological Activity of Ephedra Heterocycles, Alkaloids - Alternatives in Synthesis, Modification and Application, Vasil Georgiev and Atanas Pavlov, IntechOpen, DOI: 10.5772/67387. Available from:

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