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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67482생성일: 2026년 10월 23일

(S)-11,12,13,13a-tetrahydro-1-(hydroxymethyl)-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepin-9-one → (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde

https://huagongshe.com/ko/reaction/67482

반응식

참여 물질

역할이름HCID투입량
반응물(S)-11,12,13,13a-tetrahydro-1-(hydroxymethyl)-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepin-9-oneHCID 54004960—
촉매HCID 178418406HCID 178418406—
용매DichloromethaneHCID 6344—
생성물(S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehydeHCID 22822210—

반응 단계

A suspension of 12.1 g (45 mmol) of (S)-11,12,13,13a-tetrahydro-1-(hydroxymethyl)-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepin-9-one in 300 ml of methylene chloride is treated with 70 g of manganese dioxide and stirred at room temperature for ca 0.75 hour. After filtration over Dicalit, the filtrate is evaporated in vacuo and the residue is washed with ca 100 ml of boiling ethyl acetate. There is obtained (S)-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxaldehyde of melting point 206°-208° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346034
출처 데이터셋uspto-grants-1982_08
ORD IDord-b177a084a1a64fb49c6a8d7fcffcd3d3
출처 메모uspto-grants-1982_08