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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

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl PyrocarbonateHCID 3051—
反応物[2-[4-(Trifluoromethoxy)phenyl]-4-pyridyl]methanamineHCID 68759664—
反応物2-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acidHCID 90384201—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(4-fluorophenyl)sulfonyl-ethyl-amino]-N-[[2-[4-(trifluoromethoxy)phenyl]-4-pyridyl]methyl]prop-2-enamideHCID 7831990930%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09409864B2
出典データセットuspto-grants-2016_08
ORD IDord-c6418437146b4e93902feaae00affdcb
出典メモuspto-grants-2016_08