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HRID 1458作成日:2026年10月27日

N-methyl-2-pyrrolidone → 3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinone

https://huagongshe.com/reaction/1458

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-2-pyrrolidoneHCID 13387—
反応物Sodium TrifluoroacetateHCID 517019—
反応物3,6-diethyl-5-iodo-2-phenyl-4(3H)-pyrimidinoneHCID 19690660—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒Diethyl EtherHCID 3283—
生成物3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinoneHCID 1969072042.2%

反応手順

A mixture of 1.00 g (2.8 mmol) of 3,6-diethyl-5-iodo-2-phenyl-4(3H)-pyrimidinone, 1.08 g (5.7 mmol) of copper (I) iodide, 1.54 g (11.3 mmol) of sodium trifluoroacetate and 8 mL of anhydrous N-methylpyrrolidinone was heated at 175 C for 2 h. The mixture was cooled, diluted with 175 mL of ether, washed with four 50 mL portions of water and dried over MgSO4. Removal of the solvent on the rotovap afforded 0.92 g of crude product as a brown oil. This material was purified by flash chromatography on a 25 g column of silica gel eluting with 100 mL portions of 0, 10, 20, 30, 40, 50 and 75% ether in hexanes to afford 0.35 g of 3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinone (compound 185) as a white solid. 1H-NMR (CDCl3) 1.25(3H,t), 1.30(3H,t), 2.8(2H,q), 4.0(2H,q), 7.5(5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726124
出典データセットuspto-grants-1998_03
ORD IDord-5d84c8f338a741eebe88ed5f50eec903
出典メモuspto-grants-1998_03