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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38788생성일: 2026년 10월 25일

Pyridine → N-{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}-2-(tetrahydro-2H-pyran-4-yl)acetamide

https://huagongshe.com/reaction/38788

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Ethyl AcetateHCID 8857—
반응물(Tetrahydro-2H-pyran-4-yl)acetyl chlorideHCID 24229747—
반응물N2-(3-chlorophenyl)-4-(trifluoromethyl)pyrimidine-2,5-diamineHCID 58168950—
용매DichloromethaneHCID 6344—
생성물N-{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}-2-(tetrahydro-2H-pyran-4-yl)acetamideHCID 66720247—

반응 단계

To a mixture of N2-(3-chlorophenyl)-4-(trifluoromethyl)pyrimidine-2,5-diamine (147 mg), pyridine (62 μL), and dichloromethane (1 mL) was added a solution of the above crude tetrahydro-2H-pyran-4-ylacetyl chloride in dichloromethane (2 mL) under ice-cooling, followed by stirring at room temperature for 6 hours. To the reaction mixture was added ethyl acetate (50 mL), the organic layer was washed with a 10% aqueous citric acid solution, and then the solvent was evaporated under reduced pressure. The obtained residue was washed with warmed ethyl acetate to obtain N-{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}-2-(tetrahydro-2H-pyran-4-yl)acetamide (176 mg) as a colorless powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524727B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4f19d48c4c4c462cbb42b0573b4dd5ee
출처 메모uspto-grants-2013_09