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HRID 275931作成日:2026年10月25日

O-Toluidine → 6-Methoxymethyl-5-methyl-2-(2-methylphenylamino)-4-(1,2,3,4-tetrahydro isoquinolin-2-yl)pyrimidine hydrochloride

https://huagongshe.com/reaction/275931

反応式

関与物質

役割名称HCID仕込み量
反応物O-ToluidineHCID 7242—
反応物TriethylamineHCID 8471—
反応物6-Methoxymethyl-5-methyl-2-chloro-4-(1,2,3,4-tetrahydroisoquinolin-2-yl)pyrimidineHCID 18315787—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物6-Methoxymethyl-5-methyl-2-(2-methylphenylamino)-4-(1,2,3,4-tetrahydro isoquinolin-2-yl)pyrimidine hydrochlorideHCID 1831581032.5%

反応条件

温度130 °C

反応手順

o-Toluidine(0.48 ml, 4.5 mmol) and triethylamine were added to a solution of 6-methoxymethyl-5-methyl-2-chloro-4-(1,2,3,4-tetrahydroisoquinolin-2-yl)pyrimidine (0.9 g, 3 mmol) in dimethylformamide(5 ml) and stirred for 5 hours at 130° C. The reaction mixture was cooled to a room temperature, diluted with dichloromethane, and washed with aqueous sodium hydroxide and water. The organic layer was dried over anhydrous magnesium sulfate, concentrated, and the residual oil was purified by column chromatography. The purified compound was dissolved in ethyl ether. Ethyl ether saturated with hydrochloric acid was added to a mixture solution. The resulting solid was filtered and dried to give 400 mg of the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352993B1
出典データセットuspto-grants-2002_03
ORD IDord-305f6026270e46898cae1cd4b3176bc2
出典メモuspto-grants-2002_03