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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 268480생성일: 2026년 10월 26일

(Phenylmethyl)hydrazine → 1-benzyl-8-chloro-6-(2-chlorophenyl)-1H,4H-pyrazolo[4,3-d](2)benzazepine hydrochloride

https://huagongshe.com/reaction/268480

반응식

참여 물질

역할이름HCID투입량
반응물(Phenylmethyl)hydrazineHCID 11157—
반응물8-Chloro-1-(2-chlorophenyl)-4-dimethylaminomethylidene-3,4-dihydro-2-benzazepin-5-oneHCID 53656924—
용매EthanolHCID 702—
생성물1-benzyl-8-chloro-6-(2-chlorophenyl)-1H,4H-pyrazolo[4,3-d](2)benzazepine hydrochlorideHCID 21431636—

반응 단계

The mixture of 0.72 g of 8-chloro-1-(2-chlorophenyl)-4-dimethylaminomethylidene-3,4-dihydro-2-benzazepin-5-one, 0.64 g of benzylhydrazine and 35 ml of ethanol is refluxed for 45 minutes and evaporated under reduced pressure. The residue is taken up in 20 ml methylene chloride, the solution washed with aqueous sodium bicarbonate and stirred with 6 ml of N hydrochloric acid for 20 minutes. The aqueous solution is made basic with sodium carbonate, the mixture stirred, the organic layer separated, dried and evaporated. The residue is taken up in the minimum amount of ethanol, the solution acidified with ethereal hydrogen chloride and the precipitate formed filtered off, to yield the 1-benzyl-8-chloro-6-(2-chlorophenyl)-1H,4H-pyrazolo[4,3-d](2)benzazepine hydrochloride melting at 218°-221°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03947585
출처 데이터셋uspto-grants-1976_03
ORD IDord-8543385e927444d79dfb7e7adf8de18d
출처 메모uspto-grants-1976_03