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HRID 1667701作成日:2026年10月26日

Dimethylformamide → 4-(3-Chloro-phenyl)-2-(5-dimethoxymethyl-2-nitro-phenylamino)-thiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1667701

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Cesium carbonateHCID 10796—
反応物HCID 16658823HCID 16658823—
反応物4-Dimethoxymethyl-2-fluoro-1-nitrobenzeneHCID 54032292—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4-(3-Chloro-phenyl)-2-(5-dimethoxymethyl-2-nitro-phenylamino)-thiazole-5-carboxylic acid amideHCID 8664280847.5%

反応手順

A mixture of 3.6 g (15 mmole) of 2-amino-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid amide (V.2), 3.9 g (17.9 mmole) of 4-(dimethoxymethyl)-2-fluoro-1-nitro-benzene (IV.2a), 7.3 g (22.5 mmole) cesium carbonate, and 30 mL of dimethylformamide was heated at 70 degrees for 18 hours. The mixture was cooled, diluted with 150 mL of ethyl acetate and 100 mL of water. The ethyl acetate layer was washed once with 100 mL of brine and dried over anhydrous sodium sulfate. The mixture was filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with hexanes-ethyl acetate (50:50) to give 3.2 g of 4-(3-chloro-phenyl)-2-(5-dimethoxymethyl-2-nitro-phenylamino)-thiazole-5-carboxylic acid amide (VI.2a).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044213B2
出典データセットuspto-grants-2011_10
ORD IDord-84d4393fea4048b4a29b84a4af0a00fe
出典メモuspto-grants-2011_10