関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 4-Bromo-6,7-dihydro-8(5H)-isoquinolinone | HCID 71743380 | — |
| 触媒 | Titanium isopropoxide | HCID 11026 | — |
| 生成物 | 4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-amine | HCID 71743379 | 85% |
反応手順
4-Bromo-6,7-dihydroisoquinolin-8(5H)-one (intermediate B-11 [C]) (4.81 g, 21.3 mmol), titanium (IV) isopropoxide (12.1 g, 42.6 mmol) and ammonia, 2.0 M solution in MeOH (53.2 mL, 106 mmol) were stirred at room temperature for 5 h. The reaction was cooled to 0° C. and NaBH4 (1.21 g, 31.9 mmol) was added portionwise over 10 min; the resulting mixture was stirred at room temperature for an additional 2 h. The reaction was quenched by pouring it into aq ammonium hydroxide 25%, the precipitate was filtered and washed with EtOAc (3×, each time suspended in AcOEt and stirred for 5 min). The organic layer was separated and the remaining aqueous layer was extracted with EtOAc. The combined organic extracts were extracted with 1 M HCl. The acidic aqueous extracts were washed with ethyl acetate (1×), then treated with aqueous sodium hydroxide (2 M) to give pH 10-12 and extracted with EtOAc (3×). The combined organic extracts were washed with brine, dried (Na2SO4), and concentrated in vacuo to afford the title compound (4.11 g, 85%) as brown solid. MS: 225 (M+, 1Br).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09133158B2 |
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| 出典データセット | uspto-grants-2015_09 |
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| ORD ID | ord-43ba7f842f0f4b03953bd109086abdd0 |
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| 出典メモ | uspto-grants-2015_09 |
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