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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1698870생성일: 2026년 10월 27일

4-(2-Chloro-4-methoxyphenyl)-5-methyl-2-[N-(5-carboxy-2-methoxyphenyl)-N-propylamino]thiazole → 4-(2-Chloro-4-methoxyphenyl)-5-methyl-2-[N-(5-hydroxymethyl-2-methoxyphenyl)-N-propylamino]thiazole

https://huagongshe.com/reaction/1698870

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Chloro-4-methoxyphenyl)-5-methyl-2-[N-(5-carboxy-2-methoxyphenyl)-N-propylamino]thiazoleHCID 18322262—
반응물Dichloromethane ethylacetateHCID 21226138—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물4-(2-Chloro-4-methoxyphenyl)-5-methyl-2-[N-(5-hydroxymethyl-2-methoxyphenyl)-N-propylamino]thiazoleHCID 1832224887%

반응 단계

At 0° C., under an inert atmosphere, 1.5 g of 4-(2-chloro-4-methoxyphenyl)-5methyl-2-[N-(5-carboxy-2-methoxyphenyl)-N-propylamino]thiazole are dissolved in 11 ml of tetrahydrofuran. 5 ml of a 1 M solution of lithium aluminium hydride in tetrahydrofuran are added slowly so that the temperature of the mixture does not exceed 10° C. After 2 hours at room temperature, the reaction mixture is cooled with the aid of an ice bath and then hydrolyzed slowly. The crude material is alkalanized before being filtered over sodium sulphate. After evaporation under vacuum, the product is obtained by purification on a silica gel; eluent: dichloro-methane/ethyl acetate 95/5 (v/v); yield=87%. The expected product is in the form of a powder; m.p.=115° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06344470B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-655683a367c84e6ea45ca2a7e573eb76
출처 메모uspto-grants-2002_02