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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 596368생성일: 2026년 10월 24일

Potassium Iodide → HCID 21437288, 화합물

https://huagongshe.com/ko/reaction/596368

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium HydroxideHCID 14797—
반응물(Cyclopropylmethyl)ammonium chlorideHCID 81671—
반응물8-(trifluoromethyl)-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepineHCID 21330780—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물HCID 21437288HCID 21437288—

반응 단계

A stirred solution of potassium hydroxide (3.37 g., 0.06 mole) in methanol (30 ml.) is cooled in an ice bath, under nitrogen, and treated with (cyclopropylmethyl)-amine hydrochloride (6.45 g., 0.06 mole). The resulting mixture is kept in the ice bath for 15 minutes, treated with tetrahydrofuran (250 ml.), 8-(trifluoromethyl)-1-(chloromethyl)-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine (6.86 g., 0.02 mole) and potassium iodide (3.32 g., 0.02 mole) and kept at ambient temperature for 18 hours. The mixture is concentrated and the residue is mixed with water and extracted with methylene chloride. The extract is washed with brine, dried over anhydrous sodium sulfate and concentrated. The product is crystallized once from ethyl acetate and once from methylene chloride ethyl acetate to give 8-(trifluoromethyl)-1-[[(cyclopropylmethyl)amino]methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine. Preparation 28 8 -Chloro-1-[[(cyclopropylmethyl)amino] methyl]-6-(o-chlorophenyl)-4H-s-triazolo[4,3-a][1,4]benzodiazepine

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04010177
출처 데이터셋uspto-grants-1977_03
ORD IDord-b85af1f64e684f52a0aff5d18ad57932
출처 메모uspto-grants-1977_03