AMINEPTINE HCL

AMINEPTINE HCL 구조식 이미지
카스 번호:
30272-08-3
상품명:
AMINEPTINE HCL
동의어(영문):
s1694;Chebi:50003;AMINEPTINE HCL;amineptinehydrochloride;heptanoic acid hydrochloride;Amineptene hydrochloride(Amineptine);7-((10,11-Dihydro-5H-dibenzo[a,d][7]annulen-5-yl);7-((10,11-dihydro-5h-dibenzo(a,d)cyclohepten-5-yl)amino)-heptanoicacihydr;N-(6-Carboxyhexyl)-10,11-dihydro-5H-dibenzo[A,D]cyclohepten-5-aminium chloride;7-[(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)amino]heptanoic acid hydrochloride
CBNumber:
CB8300780
분자식:
C22H28ClNO2
포뮬러 무게:
373.92
MOL 파일:
30272-08-3.mol

AMINEPTINE HCL 속성

녹는점
226-230°

안전

AMINEPTINE HCL C화학적 특성, 용도, 생산

Originator

Survector,Eutherapie,France,1978

Manufacturing Process

6.5 g of 5-chloro-10,11-dihydro-5H-dibenzo[a,d]cycloheptene in 60 ml of nitromethane and 10.8 g of ethyl 7-aminoheptanoate in 12ml of nitromethane were mixed at ambient temperature. The reaction was slightly exothermic. The reaction mixture was left to stand overnight and the solvent was evaporated in vacuum. The residue was taken up in normal hydrochloric acid and the resulting precipitate was filtered off.
10.5 g of crude ethyl 7-[dibenzo(a,d)cycloheptadiene-5-yl]aminoheptanoate hydrochloride were obtained, of which a sample recrystallized from benzene gave a pure product melting instantaneously at 166°C to 168°C.
The hydrochloride of the crude ester obtained above was added to 25 ml of 2 N hydrochloric acid. The whole was kept under reflux for 2 hours. The material dissolved and a new hydrochloride then reprecipitated. After cooling, the hydrochloride of the crude acid was filtered off, washed with iced water and then recrystallized from distilled water. 5.7 g of 7- [dibenzo(a,d)cycloheptadienb-yl] aminoheptanoic acid hydrochloride were obtained, melting instantaneously at 226°C to 230°C.

Therapeutic Function

Central stimulant

AMINEPTINE HCL 준비 용품 및 원자재

원자재

준비 용품


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