Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434304생성일: 2026년 10월 25일
Diisopropylethylamine → (E)-N-{(S)-2-[4-(4-Fluoro-benzoyl)-piperidin-1-yl]-1-hydroxymethyl-ethyl)-3-(5-cyano-2-methoxy-phenyl)-acrylamide
https://huagongshe.com/reaction/434304
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 반응물 | (E)-3-(5-cyano-2-methoxy-phenyl)-acrylic acid | HCID 11458357 | — |
| 반응물 | [1-((S)-2-Amino-3-hydroxy-propyl)-piperidin-4-yl]-(4-fluoro-phenyl)-methanone hydrochloride | HCID 68809497 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (E)-N-{(S)-2-[4-(4-Fluoro-benzoyl)-piperidin-1-yl]-1-hydroxymethyl-ethyl)-3-(5-cyano-2-methoxy-phenyl)-acrylamide | HCID 69986033 | — |
반응 단계
To a solution of [1-((S)-2-amino-3-hydroxy-propyl)-piperidin-4-yl]-(4-fluoro-phenyl)-methanone hydrochloride (1.8 g, 5.7 mmol) and diisopropylethylamine (2.0 ml, 11.4 mmol) in dichloromethane (45 ml) is added (E)-3-(5-cyano-2-methoxy-phenyl)-acrylic acid (1.1 g, 5.7 mmol) followed by 2-(1H benzotriazol-1-yl)-1,1,3,3,-tetramethyluronium tetrafluoroborate (1.83 g, 5.7 mmol). The reaction mixture is stirred at ambient temperature for 4.5 hours, then filtered and the filtrate washed with water (50 ml), saturated sodium bicarbonate solution (50 ml), water (50 ml) and brine (50 ml). The organic phase is dried over magnesium sulphate, the solvent evaporated and the residue purified by flash silica chromatography (dichloromethane:methanol; 98:2 to 92:8 elution gradient) to afford the product, [MH]+466.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06670379B2 |
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| 출처 데이터셋 | uspto-grants-2003_12 |
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| ORD ID | ord-027795b7f3a748158af9e2b8b8b6ecbc |
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| 출처 메모 | uspto-grants-2003_12 |
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