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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414907생성일: 2026년 10월 25일

Dimethylamine → N,N-dimethyl-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxamide

https://huagongshe.com/reaction/1414907

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물IsopropanolHCID 3776—
반응물Sodium CyanideHCID 8929—
반응물6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehydeHCID 21486011—
촉매HCID 178418406HCID 178418406—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
용매Dioxane isopropanolHCID 20284604—
생성물N,N-dimethyl-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxamideHCID 21486010—

반응 단계

80 ml of isopropanol is added to 120 ml of a 20% solution of dimethylamine in dioxane. After this has cooled to 0°, additions are made, with stirring, of 3.7 g (0.075 mole) of sodium cyanide and, after 5 minutes, of a solution of 4.8 g (0.015 mole) of 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde [see Example 1 a)] in 50 ml of dioxane/isopropanol (1:1), as well as of 13 g of manganese dioxide. After 10 minutes, a further addition is made of 13 g of manganese dioxide (total 0.3 mole), and the mixture subsequently stirred for 4 hours at 0°. After the addition of methylene chloride, the reaction mixture is filtered and the filtrate concentrated by evaporation. Crystallisation of the residue from ethyl acetate/petroleum ether yields N,N-dimethyl-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxamide, M.P. 180°- 181° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04002764
출처 데이터셋uspto-grants-1977_01
ORD IDord-184ac9eff0f74e0da193870791c5a6d7
출처 메모uspto-grants-1977_01