Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131356생성일: 2026년 10월 26일
4,4,4-Trifluorobutanoic acid → N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazapin-3-yl)-4,4,4-trifluoro-butyramide
https://huagongshe.com/reaction/131356
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4,4,4-Trifluorobutanoic acid | HCID 2777085 | — |
| 반응물 | 3-amino-1H-1,5-benzodiazepine-2,4(3H,5H)-dione | HCID 21955806 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazapin-3-yl)-4,4,4-trifluoro-butyramide | HCID 58626040 | 74% |
반응 단계
Combine 3-amino-1H-1,5-benzodiazepine-2,4-(3H, 5H)-dione (5.60 g, 29.3 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimde hydrochloride (6.75 g, 35.2 mmol) and 4(dimethylamino)pyridine (0.183 g, 1.5 mmol) in 100 mL DMF, add 4,4,4-trifluoro butyric acid dropwise at 0-5° C. After addition, stir the reaction mixture at ice-water. After half an hour, warm to RT. After stirring overnight, remove solvent DMF under reduce pressure and suspend the residue in 200 mL of mixed solvent (CHCl3: i-PrOH=3:1). Collect the solid via vacuum filtration to give the title compound (6.87 g, yield 74%): mass spectrum (APCI) (m/e): 316.1 (M+1); 1H NMR (400 MHz, DMSO-d6): δ 10.72 (s, 2H), 8.60 (d, 1H, J=7.2 Hz), 7.24-7.15 (m, 4H), 4.74 (d, 1H, J=7.2 Hz), 2.58 (t, 2H, J=7.2 Hz), 2.39-2.35 (m, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07384934B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-de96973e6ca942bba5431d5ecdb42ab3 |
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| 출처 메모 | uspto-grants-2008_06 |
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