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HRID 38788作成日:2026年10月26日

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

https://huagongshe.com/reaction/38788

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Ethyl AcetateHCID 8857—
反応物(Tetrahydro-2H-pyran-4-yl)acetyl chlorideHCID 24229747—
反応物N2-(3-chlorophenyl)-4-(trifluoromethyl)pyrimidine-2,5-diamineHCID 58168950—
溶媒DichloromethaneHCID 6344—
生成物N-{2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}-2-(tetrahydro-2H-pyran-4-yl)acetamideHCID 66720247—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524727B2
出典データセットuspto-grants-2013_09
ORD IDord-4f19d48c4c4c462cbb42b0573b4dd5ee
出典メモuspto-grants-2013_09