関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Lithium Hydroxide | HCID 3939 | — |
| 反応物 | 3-(Chloromethyl)quinoline hydrochloride | HCID 14548126 | — |
| 反応物 | 3-(chloromethyl)-6-methoxy-N-(2-methoxyethyl)quinolin-2-amine hydrochloride | HCID 68182273 | — |
| 反応物 | HCID 178437769 | HCID 178437769 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 178437787 | HCID 178437787 | — |
反応手順
To a solution of 1-ethyl-6,7-dimethoxyisoquinolin-3-ol SLA 47022 (436 mg, 1.9 mmol) in THF (13 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added 3-(chloromethyl)quinoline hydrochloride SLA 47064B (400 mg, 1.9 mmol) and a 2 N aq. LiOH solution (1.90 mL, 3.80 mmol) and the mixture was stirred at 160° C. for 1.5 h under microwave irradiation. After cooling to RT, THF was removed at 40° C. under vacuum and the residue was taken up in CH2Cl2 (50 mL), washed with brine (10 mL), dried over Na2SO4, filtered, and concentrated under vacuum. Purification by column chromatography (SiO2, eluent CH2Cl2:MeOH=100:0 to 94:6) provided 1-ethyl-6,7-dimethoxy-4-(quinolin-3-ylmethyl)isoquinolin-3-ol. This free base was dissolved in MeOH (2 mL) in a 10 mL round-bottomed flask equipped with a magnetic stirrer before addition of 0.149 M HCl solution in MeOH (2.0 mL). The reaction mixture was stirred for 5 min at RT and concentrated at 40° C. under vacuum to afford 1-ethyl-6,7-dimethoxy-4-(quinolin-3-ylmethyl)isoquinolin-3-ol dihydrochloride 78 as a yellow solid (87.5 mg, 10% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08772316B2 |
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| 出典データセット | uspto-grants-2014_07 |
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| ORD ID | ord-8b07417295c641d3a3c72ee4c360d3fa |
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| 出典メモ | uspto-grants-2014_07 |
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