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HRID 2294014作成日:2026年10月25日

5,6,7,8-Tetrahydroisoquinoline → 2-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-5,6,7,8-tetrahydro-isoquinolinium chloride hydrochloride

https://huagongshe.com/reaction/2294014

反応式

関与物質

役割名称HCID仕込み量
反応物5,6,7,8-TetrahydroisoquinolineHCID 119010—
反応物5-(Chloromethyl)-2-methylpyrimidin-4-amine--hydrogen chloride (1/1)HCID 21473611—
溶媒DimethylformamideHCID 6228—
生成物2-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-5,6,7,8-tetrahydro-isoquinolinium chloride hydrochlorideHCID 2147364084%

反応手順

A suspension of 11.6 g (0.060 mol) of 5-chloromethyl-2-methyl-pyrimidin-4-ylamine hydrochloride in 40 ml of dimethyl-formamide was treated with 8.0 ml (0.060 mol) of 5,6,7,8-tetra-hydro-isoquinoline, dissolved at 120° and stirred at 800 for 16 hours. The mixture was cooled, suction filtered, washed with a small amount of dimethylformamide, then with ethyl acetate and dried in a vacuum. 16.5 g (84%) of 2-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-5,6,7,8-tetrahydro-isoquinolinium chloride hydrochloride were obtained as yellowish crystals; m.p. 242°-244°.

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-3dfc5734710d4f9f8d7c6e1180668cdf
出典メモuspto-grants-1997_11