関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | 6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine | HCID 57908192 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-chloro-2-(1-methylcyclopropyl)-1H-pyrrolo[2,3-c]pyridine | HCID 57908175 | 73% |
反応手順
To a solution of 6-chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine (3.0 g, 15 mmol) in DMF (50 mL) was added t-BuOK (3.3 g, 29 mmol) under N2 atmosphere. The mixture was heated at 80° C. overnight and quenched with H2O (100 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (50 mL×3). The combined organic layer was washed with brine, dried over anhydrous Na2SO4 and purified by chromatography on silica gel (3% EtOAc in petroleum ether) to afford 5-chloro-2-(1-methylcyclopropyl)-1H-pyrrolo[2,3-c]pyridine (2.2 g, 73%). 1H-NMR (CDCl3, 300 MHz) δ 9.79 (br s, 1H), 8.37 (s, 1H), 7.36 (s, 1H), 6.16 (s, 1H), 1.51 (s, 3H), 1.09 (m, 2H), 0.89 (m, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08563573B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-c5723815144547c3a710d8476f6c9db9 |
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| 出典メモ | uspto-grants-2013_10 |
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