PHENTERMINE HYDROCHLORIDE

PHENTERMINE HYDROCHLORIDE Basic information
Product Name:PHENTERMINE HYDROCHLORIDE
Synonyms:1-phenyl-2-methyl-2-aminopropanehydrochloride;alpha,alpha-dimethyl-phenethylaminhydrochloride;alpha-methylamphetaminehydrochloride;benzeneethanamine,alpha,alpha-dimethyl,hydrochloride;phenyl-t-butylaminehydrochloride;BenzeneethanaMine, α,α-diMethyl-, hydrochloride (1:1);NCAIGTHBQTXTLR-UHFFFAOYSA-N;Phentermine (hydrochloride) (CRM)
CAS:1197-21-3
MF:C10H16ClN
MW:185.69
EINECS:214-821-9
Product Categories:Amines;Aromatics;Aminomethyl's;Phenyls & Phenyl-Het;Intermediates & Fine Chemicals;Pharmaceuticals;Phenyls & Phenyl-Het
Mol File:1197-21-3.mol
PHENTERMINE HYDROCHLORIDE Structure
PHENTERMINE HYDROCHLORIDE Chemical Properties
Melting point 200-201℃
solubility DMF: 3 mg/ml; DMSO: 5 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 5 mg/ml
form A neat solid
Merck 13,7346
CAS DataBase Reference1197-21-3(CAS DataBase Reference)
Safety Information
Hazard Codes T,Xi
Risk Statements 25
Safety Statements 22-26-36/37-45
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS SH4950000
Hazard Note Irritant
HS Code 2921460000
Toxicitymouse,LD50,oral,154mg/kg (154mg/kg),Toxicology and Applied Pharmacology. Vol. 3, Pg. 256, 1961.
MSDS Information
ProviderLanguage
SigmaAldrich English
PHENTERMINE HYDROCHLORIDE Usage And Synthesis
Chemical PropertiesWhite Solid
OriginatorWilpo ,Dorsey, US,1961
UsesControlled substance (stimulant). Anorexic. An Amphetamine derivative.
Manufacturing ProcessPreparation of isobutyrophenone: In a 12 liter, 3-necked flask, 1,280 grams of aluminum chloride was covered with 2,000 cc of dry thiophene-free benzene and a solution of 919 grams of isobutyryl chloride, (BP 92°-94°C) in 1 liter of benzene was added slowly with stirring. After heating for 3 hours at reflux, the solution was cooled and poured over a mixture of 1 liter of concentrated hydrochloric acid and 5 kg of ice. The benzene layer was separated, the aqueous layer extracted with benzene, and the combined benzene solutions were washed, dried and concentrated in vacuo. The residue was distilled rapidly to give 1,051 grams of isobutyrophenone, boiling at 81°-89°C at 1 mm, yield 83.4%.
Preparation of 1,3-Diphenyl-2,2-Dimethylpropanone-1: Sodamide was prepared from 12.5 grams of sodium added in small portions to 600 cc of liquid ammonia with 1 gram of hydrous ferric chloride as catalyst. The ammonia was replaced by 200 cc of dry toluene and without delay a solution of 74 grams of isobutyrophenone and 76.5 grams of benzyl bromide in 200 cc of benzene was slowly added with stirring. The reaction mixture was heated on a boiling water bath for 48 hours. Water was then added, the organic layer separated and the product isolated by distillation. The 1,3-diphenyl-2,2 Phentermine dimethylpropanone-1 boiled from 142°-143°C at a pressure of 3 mm, nD201.5652.
Preparation of α,α-Dimethyl-β-Phenylpropionamide: Sodamide was prepared from 7.6 grams of sodium in 350 cc of liquid ammonia with 0.9 gram of hydrous ferric chloride. The ammonia was replaced by 250 cc of toluene, the mixture was heated to 60°C and 71.4 grams of 1,3-diphenyl-2,2-dimethyl propanone-1 dissolved in 150 cc of toluene was added. The mixture was stirred and heated on a steam bath for 5 hours. A clear red color appeared in 15 minutes and disappeared after about an hour. After cooling, water was added, the organic layer was washed, dried, and concentrated to give 36.5 grams of α,α-dimethyl-β-phenyl propionamide which crystallized slowly after the addition of an equal volume of petroleum ether. The product melted at 62°C after crystallization from benzene-petroleum ether.
Preparation of Di-(β-Phenyl-α,α-Dimethylethyl)Urea: 3.5 grams of α,αdimethyl-β-phenylpropionamide in 420 cc of water was added to a solution of 87.5 grams of potassium hydroxide and 35 grams of bromine in 350 cc of water. After 2 hours at 60°C, the product was obtained on crystallization from ethanol, melting at 184°C.
Preparation of ω-Phenyl-tert-Butylamine: 24 grams of the urea derivative obtained as indicated above, were well mixed with 96 grams of calcium hydroxide in a flask immersed in an air bath and provided with a dropping funnel the stem of which reached the bottom of the flask. The mixture was heated to 240°-260°C (inside temperature) for 7 hours during which time 86 cc of water was slowly added. The vapors were collected in a receiver cooled with ice. After extraction with ether and distillation, the product was obtained as a colorless liquid boiling from 80°-84°C at 9 mm according to US Patent 2,590,079.
The ether solution may be dried and saturated with hydrogen chloride and the precipitated hydrochloride recrystallized from a mixture of 50 parts alcohol and 100 parts of acetone.
The pure hydrochloride is thus obtained as a white crystalline substance having a MP of 195°-196°C, according to US Patent 2,408,345.





Brand nameAdipex-P(Teva); Fastin (GlaxoSmithKline).
Therapeutic FunctionAntiobesity
PHENTERMINE HYDROCHLORIDE Preparation Products And Raw materials
Raw materialsAmmonia-->Calcium hydroxide-->Isobutyryl chloride-->Hydrochloric acid-->Benzene-->Benzyl bromide-->Sodium-->Potassium hydroxide
AURORA KA-3047 DL-A-METHYL-M-TYROSINE METHYL ESTER HYDROCHLORIDE 1-(4-FLUOROPHENYL)-2-METHYL-2-AMINOPROPANE HYDROCHLORIDE cloforex ALPHA-METHYL-DL-M-TYROSINE METHYL ESTER HYDROCHLORIDE: MONOHYDRATE METHYL 1,5-DIBENZYL-3-(2-CHLOROPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE AURORA KA-3040 ALPHA-METHYL-DL-TYROSINE METHYL ESTER HYDROCHLORIDE N-(P-CHLORO-ALPHA,ALPHA-DIMETHYL PHENETHYL)UREA ALPHA-METHYL-DL-PHENYLALANINE METHYL ESTER HYDROCHLORIDE 2-(HYDROXYAMINO)-2-METHYL-1-PHENYLPROPAN-1-ONE HYDROCHLORIDE 4-(CHLOROMETHYL)-2,2-DIMETHYL-1,2-DIHYDROBENZO[F]ISOQUINOLINE METHYL 1-BENZYL-5-(4-CHLOROPHENYL)-3-(4-METHOXYPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE 1-CHLOROMETHYL-3,3-DIMETHYL-3,4-DIHYDRO-ISOQUINOLINE PHENTERMINE HYDROCHLORIDE METHYL 1,5-DIBENZYL-3-(4-CHLOROPHENYL)-4,6-DIOXOOCTAHYDROPYRROLO[3,4-C]PYRROLE-1-CARBOXYLATE TOSLAB 141649 chlorоphentermine

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