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5,6,7,8-Tetrahydroisoquinoline → 2-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-5,6,7,8-tetrahydro-isoquinolinium chloride hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5,6,7,8-Tetrahydroisoquinoline | HCID 119010 | — |
| 反応物 | 5-(Chloromethyl)-2-methylpyrimidin-4-amine--hydrogen chloride (1/1) | HCID 21473611 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-5,6,7,8-tetrahydro-isoquinolinium chloride hydrochloride | HCID 21473640 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05688798 |
| 出典データセット | uspto-grants-1997_11 |
| ORD ID | ord-3dfc5734710d4f9f8d7c6e1180668cdf |
| 出典メモ | uspto-grants-1997_11 |