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HRID 1479809作成日:2026年10月26日
Diethyl Pyrocarbonate → 2-[(4-fluorophenyl)sulfonyl-ethyl-amino]-N-[[2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methyl]prop-2-enamide
https://huagongshe.com/reaction/1479809
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diethyl Pyrocarbonate | HCID 3051 | — |
| 反応物 | [2-[4-(Trifluoromethoxy)phenyl]-4-pyridyl]methanamine | HCID 68759664 | — |
| 反応物 | 2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acid | HCID 90384201 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-[(4-fluorophenyl)sulfonyl-ethyl-amino]-N-[[2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methyl]prop-2-enamide | HCID 78319909 | 30% |
反応手順
A solution of acid 4B (0.25 g, 1 mmol) in THF (20 mL) was added with DEPC (0.17 mL, 1.3 mol eq) and the mixture was stirred at room temperature for about 5 minutes. Then [2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methanamine 21B (0.27 g, 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, the residue was suspended in EtOAc (30 mL) and washed with water (50 mL) and brine. The separated organic phase, after drying over Na2SO4, was evaporated under reduced pressure and the residue purified by flash chromatography (7:3 EtOAc:Petroleum ether) to afford a pale orange solid (0.12 g) after crystallization from a mixture of diethyl ether/petroleum ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09409864B2 |
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| 出典データセット | uspto-grants-2016_08 |
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| ORD ID | ord-c6418437146b4e93902feaae00affdcb |
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| 出典メモ | uspto-grants-2016_08 |
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