Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 440047생성일: 2026년 10월 26일
Triethylamine → 6,7-dihydro-5-(2-chloro-4-nitrobenzoyl)-5H-pyrrolo[1,2-a][1,5]benzodiazepine
https://huagongshe.com/reaction/440047
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzoyl chloride, 2-chloro-4-nitro- | HCID 81522 | — |
| 반응물 | 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepine | HCID 12359341 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 6,7-dihydro-5-(2-chloro-4-nitrobenzoyl)-5H-pyrrolo[1,2-a][1,5]benzodiazepine | HCID 21837030 | 105.6% |
반응 단계
To a solution of 0.28 g of 6,7-dihydro-5H-pyrrolo-[1,2-a][1,5]benzodiazepine in 6 ml of methylene chloride is added 0.30 g of triethylamine followed by 0.50 g of 2-chloro-4-nitrobenzoyl chloride in 0.5 ml of methylene chloride. The reaction mixture is stirred at room temperature for 1 hour then quenched with 5 ml of saturated NaHCO3. The methylene chloride is evaporated in vacuo and the residue is diluted with 5 ml of water and extracted with 20 ml of ethyl acetate. The organic layer is separated, washed with saturated NaHCO3 and brine, dried with Na2SO4 and evaporated in vacuo to give 0.59 g of a yellow foam which is triturated with ether-hexanes to give 0.56 g of the desired product as off-white solid. MS(CI): 368(M+H) (Cl35) 370(M+H) (Cl37)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05516774 |
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| 출처 데이터셋 | uspto-grants-1996_05 |
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| ORD ID | ord-1bfa38b3758b4decbcfcf30ec56ede1d |
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| 출처 메모 | uspto-grants-1996_05 |
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