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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1420013생성일: 2026년 10월 24일

Triethylamine → 9,10-Dihydro-10-(4-nitrobenzoyl)-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine

https://huagongshe.com/ko/reaction/1420013

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Nitrobenzoyl chlorideHCID 8502—
반응물9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepineHCID 21837159—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물9,10-Dihydro-10-(4-nitrobenzoyl)-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepineHCID 21837151—

반응 단계

To a solution of 10 mmol of 9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine in 50 ml of methylene chloride under argon is added 15 mmol of triethylamine followed by ice bath cooling. A solution of 11 mmol of 4-nitrobenzoyl chloride in 10 ml of methylene chloride is added dropwise. Following complete addition, the ice bath is removed and the reaction mixture stirred at room temperature for 2 hours. The volatiles are removed in vacuo to give a residue which is dissolved in ethyl acetate. The solution is washed with water, 1N HCl, NaHCO3, and brine. The organic layer is dried with Na2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography on silica gel to give desired product as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05889001
출처 데이터셋uspto-grants-1999_03
ORD IDord-87c86ea69c954bf093b95f0a0f119d54
출처 메모uspto-grants-1999_03