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HRID 2294006作成日:2026年10月25日

1,2,3,4-Tetrahydroisoquinoline → 5-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine

https://huagongshe.com/reaction/2294006

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,4-TetrahydroisoquinolineHCID 7046—
反応物TriethylamineHCID 8471—
反応物5-(Chloromethyl)-2-methylpyrimidin-4-amine--hydrogen chloride (1/1)HCID 21473611—
溶媒DimethylformamideHCID 6228—
生成物5-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamineHCID 2147365769%

反応手順

A suspension of 0.80 g (0.0041 2 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine hydrochloride in 17 ml of dimethylformamide was treated with 1.7 ml (0.0123 mol) of triethylamine and 0.67 g (5.3 mol) of 1,2,3,4-tetrahydroisoquinoline and the mixture was stirred at room temperature under argon for 3 hours. The mixture was completely freed from the solvents and the residue was chromatographed over silica gel with dichloromethane/methanol 9:1 as the eluent and recrystallized from ethyl acetate/diethyl ether. 0.72 g (69%) of 5-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)-2-methyl-pyrimidin-4-ylamine was obtained as beige crystals; m.p. 150°-153°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05688798
出典データセットuspto-grants-1997_11
ORD IDord-b49900f2135746dbbcc56e1dcb04e246
出典メモuspto-grants-1997_11