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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290951생성일: 2026년 10월 26일

Cyclohexanethiol → 10,11-Dihydro-10-[[6-(cyclohexylthio)-3-pyridinyl]carbonyl]-5H-pyrrolo-[2,1-c][1,4]benzodiazepine

https://huagongshe.com/reaction/1290951

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanethiolHCID 15290—
반응물Sodium hydrideHCID 24758—
반응물2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
반응물10-[(6-Chloro-3-pyridinyl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 21947725—
용매TetrahydrofuranHCID 8028—
생성물10,11-Dihydro-10-[[6-(cyclohexylthio)-3-pyridinyl]carbonyl]-5H-pyrrolo-[2,1-c][1,4]benzodiazepineHCID 18917474—

반응 단계

To a suspension of 35 mg of sodium hydride (60% in oil) in 3 ml of tetrahydrofuran is added under argon 0.10 g of cyclohexylmercaptan. A white precipitate forms and after 0.5 hour at room temperature, 1 ml of N,N'-dimethylpropyleneurea is added. To the mixture is added 0.13 g of 10-[(6-chloro-3-pyridinyl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine in 2 ml of tetrahydrofuran. The mixture is stirred at room temperature for 18 hours, quenched with water and ammonium chloride and concentrated under vacuum. The aqueous suspension is filtered and the solid washed with water and hexane. The solid is purified by chromatography on silica gel prep-plates with ethyl acetate-hexane (1:4) as eluent to give 0.13 g of white solid; mass spectrum (CI): 404 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05753648
출처 데이터셋uspto-grants-1998_05
ORD IDord-5694eb32bd034aefa17df9f027773f7c
출처 메모uspto-grants-1998_05