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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182618생성일: 2026년 10월 27일

Benzenepropanoic acid → N-[4-(3-chlorophenyl)-6-methyl-2-(methylthio)-5-pyrimidinyl]-3-phenylpropanamide

https://huagongshe.com/reaction/1182618

반응식

참여 물질

역할이름HCID투입량
반응물Benzenepropanoic acidHCID 107—
반응물PyridineHCID 1049—
반응물DimethylformamideHCID 6228—
반응물4-(3-Chlorophenyl)-6-methyl-2-(methylthio)-5-pyrimidinamineHCID 17854576—
용매Thionyl ChlorideHCID 24386—
생성물N-[4-(3-chlorophenyl)-6-methyl-2-(methylthio)-5-pyrimidinyl]-3-phenylpropanamideHCID 58981790—

반응 단계

51.4 mg (0.342 mmol) of 3-phenylpropionic acid was dissolved in 1 ml of thionyl chloride. A catalytic amount of DMF was added and stirred at room temperature for 3 hours. After the solvent was evaporated under reduced pressure, 45.4 mg (0.171 mmol) of 4-(3-chlorophenyl)-6-methyl-2-(methylthio)-5-pyrimidinamine and 1 ml of pyridine were added and stirred at 50° C. overnight. After the solvent was evaporated under reduced pressure, the reaction mixture was diluted with ethyl acetate and washed with saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=10/1 to 1/1) to obtain the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07288544B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-66f52f258fbd4456b5b8f6c5ff0a6088
출처 메모uspto-grants-2007_10