Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3532생성일: 2026년 10월 24일
Triethylamine → N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamide
https://huagongshe.com/ko/reaction/3532
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-[(2-methylbenzoyl)amino]benzoyl Chloride | HCID 10707441 | — |
| 반응물 | 9,10-Dihydro-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine | HCID 21836966 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-(4H-Furo[2,3-e]pyrrolo[1,2-a][1,4]-diazepin-10(9H)-ylcarbonyl)phenyl]-2-methyl benzamide | HCID 21837211 | — |
반응 단계
To a mixture of 1.1 mmol of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 10 ml of methylene chloride, cooled to 0° C. is added 1.5 mmol of triethylamine. To the mixture is added 1 mmol of 9,10-dihydro-4H-furo[2,3-e]pyrrolo[1,2-a][1,4]diazepine and the mixture stirred at room temperature for 2 hours. The reaction mixture is concentrated in vacuo and the residue is dissolved in 100 ml of ethyl acetate and washed with water, 2N citric acid, aqueous NaHCO3 and brine. The solution is dried with Na2SO4 and the volatiles concentrated in vacuo to give a solid which is purified by flash chromatography to give the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05733905 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-5f938858357146d8a8d932bcaf02b969 |
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| 출처 메모 | uspto-grants-1998_03 |
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