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HRID 390709作成日:2026年10月26日

Cesium carbonate → (NZ)-N-[5-methyl-3-(4-methylsulfanylphenyl)-1,3-thiazol-2-ylidene]pyrrolidine-1-carboxamide

https://huagongshe.com/reaction/390709

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-BromothioanisoleHCID 66037—
反応物5-Chloro-1,10-phenanthrolineHCID 77865—
反応物N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamideHCID 47197229—
反応物Water ammonium hydroxideHCID 86589665—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(NZ)-N-[5-methyl-3-(4-methylsulfanylphenyl)-1,3-thiazol-2-ylidene]pyrrolidine-1-carboxamideHCID 42644648—

反応条件

温度120 °C

反応手順

To a 4 mL vial equipped with a septum cap and stir bar was added N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamide (50 mg, 0.24 mmol), copper(I) trifluoromethanesulfonate benzene complex (23.8 mg, 0.05 mmol), 5-chloro-1,10-phenanthroline (20.3 mg, 0.09 mmol) and cesium carbonate (84.8 mg, 0.26 mmol). The mixture was placed under a nitrogen atmosphere. (4-Bromophenyl)(methyl)sulfane (0.28 mmol) in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the mixture. The reaction mixture was heated at 120° C. for overnight. A solution of concentrated ammonium hydroxide/water (1:2, 1 mL) was added and the mixture was filtered and solvent removed under reduced pressure. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383657B2
出典データセットuspto-grants-2013_02
ORD IDord-1cc60547cd994901bce749ede1d15e81
出典メモuspto-grants-2013_02