Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479874생성일: 2026년 10월 25일
Diethyl Pyrocarbonate → 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-morpholino-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide
https://huagongshe.com/reaction/1479874
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Pyrocarbonate | HCID 3051 | — |
| 반응물 | 2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acid | HCID 90384201 | — |
| 반응물 | [2-Morpholino-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine | HCID 90390699 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-morpholino-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide | HCID 90390231 | 12% |
반응 단계
A solution of acid 4B (0.40 g, 1.46 mmol) in THF (20 mL) was added with DEPC (0.28 mL, 1.3 mol eq) and the mixture was stirred at room temperature several minutes. Then [2-morpholino-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 27B (530 mg, 1.1 mol eq) and a catalytic amount of TEA were added, then the reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, water was added to the residue that is extracted with EtOAc (3×30 mL) and washed with brine (1×40 mL). The separated organic phase was dried over Na2SO4, evaporated to dryness and the residue was purified by flash chromatography (6/4 EtOAc/Petroleum ether) to afford a white solid (95 mg) after crystallization from ethyl ether. Yield=12%. 1HNMR (DMSO, 200 MHz) δ 1.087 (t, 3H, J=7.8), 3.39 (q, 2H, J=7.6), 3.55 (m, 4H), 3.71 (m, 4H), 4.42 (d, 2H, J=6.2), 5.13 (s, 1H), 6.12 (s, 1H), 6.85 (s, 1H), 7.35 (s, 1H), 7.47 (t, 2H, J=8), 7.83-7.90 (m, 4H), 8.26 (d, 2H, J=8), 8.80 (bt, 1H). [M+1] 592.33 (C28H28F4N4O4S requires 592.60).
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-e4708b418ba5452d9d9d754b0fab0fe0 |
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| 출처 메모 | uspto-grants-2016_08 |
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