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HRID 70285作成日:2026年10月24日

Dimethylformamide → 2-Bromo-1,3-thiazole-4-carboxamide

https://huagongshe.com/ja/reaction/70285

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Ammonium HydroxideHCID 14923—
反応物Thionyl ChlorideHCID 24386—
反応物2-Bromo-1,3-thiazole-4-carboxylic acidHCID 2763209—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物2-Bromo-1,3-thiazole-4-carboxamideHCID 45789632—

反応手順

To a suspension of 2-bromo-1,3-thiazole-4-carboxylic acid (3.82 g, 18.4 mmol) and a catalytic amount of DMF in CH2Cl2 (100 mL) at 0° C. was slowly added thionyl chloride (14 mL of a 2M solution in CH2Cl2). The resulting mixture was stirred for 12 h at the room temperature and then heated to reflux for 1 h. The mixture was concentrated to dryness in vacuo. The white solid obtained was taken up in ethyl acetate, added to a pre-cooled (0° C.) 9-10% aqueous ammonium hydroxide solution (90 ml) and stirred for 1 h at 0° C. The organic layer was separated and the aqueous phase was extracted twice with ethyl acetate. The combined ethyl acetate solution was washed with brine, dried over magnesium sulfate and concentrated in vacuo, affording the title compound was obtained as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.60 (s, 1 H), 7.82 (s, 1 H), 8.22 (s, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822518B2
出典データセットuspto-grants-2014_09
ORD IDord-df20cd9eadec4bdb92e112be6df54478
出典メモuspto-grants-2014_09