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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1667701생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1667701

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Cesium carbonateHCID 10796—
반응물HCID 16658823HCID 16658823—
반응물4-Dimethoxymethyl-2-fluoro-1-nitrobenzeneHCID 54032292—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4-(3-Chloro-phenyl)-2-(5-dimethoxymethyl-2-nitro-phenylamino)-thiazole-5-carboxylic acid amideHCID 8664280847.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08044213B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-84d4393fea4048b4a29b84a4af0a00fe
출처 메모uspto-grants-2011_10