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HRID 1015638作成日:2026年10月27日

Cesium carbonate → 3-Cyclopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1015638

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CyclopropylamineHCID 69828—
反応物Binap, (A+-)-HCID 634876—
反応物Methyl 3-bromo-5-phenyl-thiophene-2-carboxylateHCID 20775762—
溶媒TolueneHCID 1140—
生成物3-Cyclopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 2077576422%

反応条件

温度110 °C

反応手順

To a solution of 3-Bromo-5-phenyl-thiophene-2-carboxylic acid methyl ester (250 mg, 0.89 mmol) in toluene (25 ml) was added cyclopropylamine (57 mg, 1.0 mmol), cesium carbonate (382 mg, 1.2 mmol), BINAP (50 mg, 0.08 mmol) and tris (dibenzyli-denacetone)dipaladium (0) (38 mg, 0.04 mmol). The reaction mixture was stirred for 16 h at 110° C. in a sealed tube. The mixture was partitioned between toluene (20 mL) and water (20 mL) and the organic layer was separated. The aqueous phase was washed twice with toluene (2×10 mL) and the combined toluene layer was dried (MgSO4), concentrated and the residue was purified by preparative chromatography (10% EtOAc/Hexane) to obtain 52 mg (22%) of 3-Cyclopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester. NMR 1H (CDCl3, 400 MHz): 7.67-7.62 ppm (m, 2H, Haro); 7.43-7.32 ppm (m, 3H, Haro); 7.16 ppm (s, 1H, Haro); 3.82 ppm (S, 3H); 2.65 ppm (m, 1H); 0.62 ppm (m, 2H); 0.35 ppm (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07985769B2
出典データセットuspto-grants-2011_07
ORD IDord-78c2b097b9ca481783350ce25cc76f74
出典メモuspto-grants-2011_07