Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479803생성일: 2026년 10월 26일
Diethyl Pyrocarbonate → 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide
https://huagongshe.com/reaction/1479803
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Pyrocarbonate | HCID 3051 | — |
| 반응물 | [2-(4-Trifluoromethyl-phenyl)-pyridin-4-yl]methylamine | HCID 68758847 | — |
| 반응물 | 2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acid | HCID 90384201 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide | HCID 78324601 | 19.7% |
반응 단계
Acid 4B (273.28 mg, 1 mmol) was dissolved in 10 ml of THF and at rt DEPC (1.1 equiv, 0.15 ml) and [2-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 21A (1.1 equiv., 277.5 mg) were added to the solution. The mixture was stirred at rt overnight then evaporated. The residue was dissolved in AcOEt (30 ml) and washed with water (1×20 ml) and brine. The organic phase was dried over sodium sulfate and concentrated under vacuum. The purification of the crude by chromatographic column (EtOAc 1/petroleum ether 1) afforded 100 mg of a white solid. Yield=19% 1HNMR (DMSO, 400 MHz) δ 1.09 (3H, t, J=7.2 Hz), 3.39 (2H, q, J=6.8 Hz), 4.48 (2H, d, J=6 Hz), 5.15 (1H, s), 6.14 (1H, s), 7.36 (1H, dd, J=4.8 Hz, J′=1.2 Hz), 7.47 (2H, t, J=8.8 Hz), 7.84 (4H, m), 8.01 (1H, s), 8.30 (2H, d, J=8 Hz), 8.64 (1H, dd, J=5.2 Hz, J′=0.8 Hz), 8.89 (1H, bt) [M+1] 508.7 (C24H21F4N3O3S requires 507.50).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09409864B2 |
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| 출처 데이터셋 | uspto-grants-2016_08 |
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| ORD ID | ord-6138cc1de4934b42858f387fb8a57c70 |
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| 출처 메모 | uspto-grants-2016_08 |
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