関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | 5-Chloro-3-((trimethylsilyl)ethynyl)pyridin-2-amine | HCID 24729465 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 溶媒 | Sodium chloride; water | HCID 57417360 | — |
| 生成物 | 5-Chloro-1H-pyrrolo[2,3-b]pyridine | HCID 24229213 | — |
反応手順
Under a nitrogen atmosphere, to a solution of potassium tert-butoxide (4.0 g, 0.036 mol) in 1-methyl-2-pyrrolidone (8.0 mL) which stirred with heating at 80° C., a solution of 2-amino-5-chloro-3-[(trimethylsilyl)ethynyl]pyridine (4.0 g, 0.018 mol) in 1-methyl-2-pyrrolidone (22 mL) was added dropwise and the mixture was stirred for 1 h. Cooled to ambient temperature, the reaction mixture was diluted with brine and stirred, then extracted with diethyl ether for 3 times. The organic layer was washed with brine, dried over sodium sulfate and concentrated to afford 5-chloro-7-azaindole as solid (2.3 g, y. 85%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08742113B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-1c9338128f2b4d4896b90c169b620e39 |
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| 出典メモ | uspto-grants-2014_06 |
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