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2-Phenethylamines

Although Strike found most of these articles on Strike s own, our good friend and learned scholar Osmium emailed Strike some of the above group s articles and quite a few more that we will get at in just a bit. The following methods can be read about in the original articles in which they were published [49-51]. But there is a nice review by the same authors in which a representative example of each of their methods is included [52]. The following were taken from that review. X and speed chemists just substitute an equimolar amount of their respective p-Nitropropene for the one in the methods below. Also, it should be obvious that these reduction methods will work just fine on 2CB and other phenethylamine intermediates. [Pg.138]

Synthesis of Alkviamines. General Procedures. Method (A). The synthesis of p-phenethylamine is representative. A flame dried, nitrogen-flushed, 100 ml flask, equipped with a septum inlet, magnetic stirring bar and reflux condenser ivas cooled to 0°C. Sodium borohydride (9.5 mmol, 0.36 g) was placed in the flask followed by sequential addition of THF (13-15 ml) and BF3-Et20 (12 mmol, 1.5 ml) at 0°C. After the addition, the ice bath was removed and the contents were stirred at room temperature for 15 min. The solution... [Pg.139]

This is the branch-poiat differentiatiag phenylalanine (25, R = H) from tyrosiae (25, R = OH). Both phenylalanine and tyrosiae contain an aryl ring, a three-carbon side chain (a Cg—Cg fragment), and a nitrogen. Decarboxylation yields a two-carbon side chain (a Cg—Cg fragment), eg, 2-phenethylamine (59, R = H) from phenylalanine and tyramine (59, R = OH) from tyrosiae, although it is not certain that ia all cases decarboxylation must precede use ia alkaloid constmction. [Pg.540]

Compounds available in the United States are Hsted in Table 1. Whereas they vary in degree, all of them share similar HabiUties of cardiovascular side effects, the potential for central nervous system (CNS) stimulation, the development of tolerance, and abuse potential. AH, with the exception of ma2indol, are derivatives of phenethylamine. The introduction of an oxygen atom on the -carbon of the side chain tends to reduce CNS stimulant properties without decreasing the anorectic activity. Following the Federal Controlled Dmg Act of 1970, dmgs were classified into one of five schedules according to medical utiUty and abuse potential. [Pg.216]

BISCHLER NAPIERALSKI Isoquinoline synthesis Isoqutnoline synthesis Irom amides of phenethylamines... [Pg.36]

Isequinoline synthesis Irom aromatic aldehydes and an aminoacetal (Pomeranz-Frttsch) or from phenethylamines and glyonal acetal (Schlitter-Muller). [Pg.303]

In 1911, Ame Pictet and Theodor Spengler reported that P-arylethyl amines condensed with aldehydes in the presence of acid to give tetrahydroisoquinolines. Phenethylamine 6 was combined with dimethoxymethane 7 and HCl at elevated temperatures to give tetrahydroisoquinoline 8. Soon after, the Pictet-Spengler reaction became the standard method for the formation of tetrahydroisoquinolines. [Pg.469]

Stereoselectivity in the condensation reaction of 2-arylethylamines with carbonyl compounds to give 1,2,3,4-tetrahydroisoquinoline derivatives was somewhat dependent on whether acid catalysis or superacid catalysis was invoked. Particularly in the cases of 2-alkyl-N-benzylidene-2-phenethylamines, an enhanced stereoselectivity was observed with trifluorosulfonic acid (TFSA) as compared with the weaker acid, trifluoroacetic acid (TFA). Compound 43 was cyclized in the presence of TFA to give modest to good transicis product ratios. The analogous compound 44 was cyclized in the presence of TFSA to give slightly improved transicis product ratios. [Pg.475]

Model studies directed toward the synthesis of Ecteinascidin 743 employed an elegant Pictet-Spengler cyclization of phenethylamine 54 and the 1,2-dicarbonyl compound 55 to assemble the spiro tetrahydroisoquinoline 56 in a stereospecific fashion. " The silica-catalyzed condensation reaction provided 56 in excellent yield. [Pg.477]

The A-substituted derivatives of 4-oxo-4//-pyrido[l,2-n]pyrimidine-3-carboxamides and -3-acetamides and l,6-dimethyl-4-oxo-1,6,7,8-tetrahy-dro-4//-pyrido[l,2-n]pyrimidine-3-carboxamide were prepared by treatment of the appropriate 3-carboxylic acids and acetic acid, first with an alkyl chloroformate in the presence ofNEt3 in CHCI3 below — 10°C, then with an amine (98ACH515). A-Phenethyl and A-[2-(3,4-dimethoxyphenyl)ethyl] derivatives of 6-methyl-6,7,8,9-tetrahydro-4//-pyrido[l, 2-n]pyrimidine-3-acetamide were obtained in the reaction of 6-methyl-6,7,8,9-tetrahydro-4//-pyrido[l,2-n]pyrimidine-3-acetic acid and phenethylamines in boiling xylene under a H2O separator. Hydrazides of 4-oxo-4//- and 4-oxo-6,7,8,9-tetrahydro-4//-pyrido[l, 2-n]pyrimidine-3-acetic acid were prepared from the appropriate ester with H2NNH2 H2O in EtOH. Heating 4-oxo-4//- and 6-methyl-4-oxo-6,7,8,9-tetrahydro-4//-pyrido[l, 2-n]pyrimidine-3-acetic hydrazides in EtOH in the presence of excess Raney Ni afforded fhe appropriafe 4-oxo-6,7,8,9-fefrahydro-4//-pyrido[l,2-n]pyrimidine-3-acefa-mide. In the case of the 4-oxo-4// derivative, in addition to N-N bond... [Pg.216]

Yet another example of a so-called pharmacophoric group is the biguanide functionality, a grouping associated with oral antidiabetic activity (see the section on sulfonylureas for a fuller discussion of this activity). Condensation of 2-phenethylamine with dicyanamide affords directly the orally active hypoglycemic agent phenformin (88). ... [Pg.75]

Finally, attachment of a rather complex side chain to the para position of the benzene ring on the sulfonamide leads to the very potent, long-acting oral antidiabetic agent, glyburide (215). Preparation of this compound starts with the chlorosul-fonation of the acetamide of 3-phenethylamine (209). The resulting sulfonyl chloride (210) is then converted to the sulfonamide (211) and deacylated (212). Reaction with the salicylic acid derivative, 213, in the presence of carbodiimide affords the amide, 214. Condensation of that with cyclohexylisocyanate affords glyburide (215). ... [Pg.139]

Although the morpholine ring is often used as a modified version of a tertiary nitrogen, the ring system finds only rare use as a nucleus for medicinal agents. Both compounds below, in fact, may be regarded as more properly related to cyclized forms of hydroxy-phenethylamines. [Pg.260]

Figure 11.14 Analysis of amphetamines by GC-NPD following HS-SPME exti action from human hair (a) Normal hair (b) normal hair after addition of amphetamine (1.5 ng) and methamphetamine (16.1 ng) (c) hair of an amphetamine abuser. Peak identification is as follows 1, a-phenethylamine (internal standard) 2, amphetamine 3, methamphetamine 4, N-propyl-/3-phenethyamine (internal standard). Reprinted from Journal of Chronatography, B 707,1. Koide et ai, Determination of amphetamine and methamphetamine in human hair by headspace solid-phase microextraction and gas cliromatography with niti ogen-phosphoms detection, pp. 99 -104, copyright 1998, with permission from Elsevier Science. Figure 11.14 Analysis of amphetamines by GC-NPD following HS-SPME exti action from human hair (a) Normal hair (b) normal hair after addition of amphetamine (1.5 ng) and methamphetamine (16.1 ng) (c) hair of an amphetamine abuser. Peak identification is as follows 1, a-phenethylamine (internal standard) 2, amphetamine 3, methamphetamine 4, N-propyl-/3-phenethyamine (internal standard). Reprinted from Journal of Chronatography, B 707,1. Koide et ai, Determination of amphetamine and methamphetamine in human hair by headspace solid-phase microextraction and gas cliromatography with niti ogen-phosphoms detection, pp. 99 -104, copyright 1998, with permission from Elsevier Science.
Chemical Name 3,4-Dihydroxy-N-[3-(4-hvdroxyphenvl)-1-methvlpropyll -/3-phenethylamine Common Name —... [Pg.532]

To the reduction mixture was then added 3.5 g of 5% palladium on carbon catalyst and the mixture was hydrogenated under a hydrogen pressure of 50 psi at room temperature for 12 hours. The catalyst was removed by filtration and the filtrate was evaporated to a small volume. The concentrated filtrate was dissolved in diethyl ether and the ethereal solution was saturated with anhydrous hydrogen chloride. The reduction product, 3,4-dimethoxy-N-[3-4-methoxyphenyl)-1 -methyl-n-propy 11 phenethylamine was precipitated as the hydrochloride salt. The salt was filtered and recrystallized from ethanol melting at about 147°C to 149°C. [Pg.533]

The thermal condensetion of p-benzyloxyphenylacetic acid and of 3-methoxy-4-hydroxy-phenethylamine occurs and gives, with a yield of 86% to 92%, the N-(3-methoxy4-hydroxy-phenethyl-p-benzyloxyphenylacetamide from this latter, by cyclization according to Bischler-Napieralski with phosphorus oxychloride in acetonitrile, followed by reduction with sodium borohydride, there is obtained with a yield of 75% to 80% the 1-(p-benzyloxybenzyl)-6-meth-oxy-7-hydroxy-1,2,3,4-tetrahydroisoquinoline, which is methylated with formaldehyde and formic acid giving 1 (p-benzyloxybenzyl)-2-methyl-6-methoxy-7-hydroxy-1,2,3,4-tetrahydro-isoquinoline with a yieid of 90%. [Pg.727]

Addition of Grignard and organolithium reagents to imines 2. derived from enantiomerically pure (S)-valinol (1), provides a-substituted phenethylamines 3 in moderate to good yield and excellent diastereoselectivity (in each case only one diastereomer can be detected by NMR)15. By appropriate selection of imine and organometallic reagent both diastereomeric amines are accessible (see also refs 16 and 17). [Pg.686]

ACYLAMIDOALKYL ACETOPHENONES FROM SUBSTITUTED PHENETHYLAMINES 2-(2-ACETAMIDOETHYL)-4,5-DIMETHOXYACETOPHENONE... [Pg.3]

This is a rare transformation. The reaction of 5-phenethylamine and the bis-sulfonyl chloride of 1,2-benzenesulfonic acid, followed by KNO2 and 18-crown-6 gave R-phenethyl alcohol in 70% yield and 40% enantiomeric excess (ee). ... [Pg.494]

T. Fujita and T. Ban, Structure-activity study of phenethylamines as substrates of biosynthetic enzymes of sympathetic transmitters. J. Med. Chem., 14 (1971) 148-152. [Pg.418]

MDMA is believed to have unique psychoactive properties that clearly distinguish it from hallucinogenic or psychostimulant phenethylamines. Not only have MDMA users consistently reported this distinctiveness, but subsequent studies of MDMA and similar compounds, in many laboratories, have shown that they do not fit within the structure-activity relationships that presently are understood to define the hallucinogenic amphetamines. [Pg.2]


See other pages where 2-Phenethylamines is mentioned: [Pg.139]    [Pg.193]    [Pg.745]    [Pg.563]    [Pg.252]    [Pg.65]    [Pg.679]    [Pg.680]    [Pg.218]    [Pg.476]    [Pg.62]    [Pg.75]    [Pg.34]    [Pg.688]    [Pg.693]    [Pg.1044]    [Pg.1044]    [Pg.1045]    [Pg.177]    [Pg.412]    [Pg.226]    [Pg.132]    [Pg.58]    [Pg.60]    [Pg.63]    [Pg.3]    [Pg.7]   
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2- phenethylamin

2-Phenethylamines appetite suppressants

2-Phenethylamines structure-activity relationships

3,4-Dimethoxy- -phenethylamine

3- Methoxy phenethylamine

A-phenethylamine

Aldehydes, reaction with phenethylamines

Amines Phenethylamines

Amines phenethylamine

Asymmetric induction, with phenethylamine

Auxiliaries, chiral phenethylamine

Isoquinolines => phenethylamines

Isoquinolines from phenethylamines

JS-Phenethylamine

P-Phenethylamine

Phencyclidine 3-Phenethylamines

Phenethylamine

Phenethylamine

Phenethylamine V Phenmenthol

Phenethylamine alkaloids

Phenethylamine alkaloids Cacti

Phenethylamine alkaloids Mescaline

Phenethylamine alkaloids Peyote

Phenethylamine and Isoquinoline Alkaloids

Phenethylamine auxiliary

Phenethylamine derivatives

Phenethylamine hydrochloride

Phenethylamine moiety

Phenethylamine, 3,4,5-Trimethoxy

Phenethylamine, V-acetylaldol reaction

Phenethylamine, V-acetylaldol reaction diastereofacial preference

Phenethylamine, V-acetylaldol reaction diastereoselectivity

Phenethylamine, acetylation

Phenethylamine, reaction with

Phenethylamine, reaction with ketones

Phenethylamines Amphetamine Family

Phenethylamines Found in Plants

Phenethylamines analysis

Phenethylamines and simple isoquinolines

Phenethylamines biological effects

Phenethylamines biosynthesis

Phenethylamines by L. Reti

Phenethylamines determination

Phenethylamines diastereoselectivity

Phenethylamines occurrence

Phenethylamines reaction

Phenethylamines structure

Phenethylamines synthesis

Phenethylamines, brominated

Reduction, by amalgamated zinc and benzylcyanide to phenethylamine

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