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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48358생성일: 2026년 10월 23일

N,N,N',N'-Tetramethylazodicarboxamide → (E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-(2-thenyloxy)-1H-1,4-benzodiazepine

https://huagongshe.com/ko/reaction/48358

반응식

참여 물질

역할이름HCID투입량
반응물N,N,N',N'-TetramethylazodicarboxamideHCID 4278—
반응물TributylphosphineHCID 13831—
반응물2-ThiophenemethanolHCID 69467—
반응물(E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-8-ol hydrochlorideHCID 136386027—
용매TetrahydrofuranHCID 8028—
생성물(E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-(2-thenyloxy)-1H-1,4-benzodiazepineHCID 698919476.8%

반응 조건

온도0 °C

반응 단계

To a stirred solution of 50 mg (0.14 mmol) of (E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-1H-1,4-benzodiazepin-8-ol (prepared as described in Example 157) in 5 ml of dry tetrahydrofuran was added 0.014 ml (0.14 mmol) of thiophene-2-methanol and 0.053 ml (0.21 mmol) of tributylphosphine. The solution was cooled, under an atmosphere of nitrogen, to 0° C. and 37 mg (0.21 mmol) of 1,1′-azobis(N,N-dimethylformamide) was added. The mixture was allowed to warm up to room temperature and then stirred for 16 hours. A further 0.053 ml (0.21 mmol) of tributylphosphine and 37 mg (0.21 mmol) of 1,1′-azobis(N,N-dimethylformamide) were added and the mixture stirred for a further 4 hours. The mixture was filtered and the filtrate evaporated and then chromatographed on silica gel using dichloromethane/methanol (98:2) for the elution. There was obtained 4.2 mg of (E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-(2-thenyloxy)-1H-1,4-benzodiazepine as an orange gum MS: m/e 442.8 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06703387B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-4eb73e187bc04dcc947e0c7b5301221a
출처 메모uspto-grants-2004_03