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Triethylamine → N-(6-bromo-2-pyridinyl)-3-methylbut-2-enamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 3-Methyl-2-butenoyl chloride | HCID 102394 | — |
| 反応物 | 2-Amino-6-bromopyridine | HCID 300809 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(6-bromo-2-pyridinyl)-3-methylbut-2-enamide | HCID 43520526 | — |
反応手順
To a solution of 2-amino-6-bromopyridine (3.015 g, 0.017 mol) and Et3N (2.40 mL, 0.017 mol) in CH2Cl2 (20.0 mL), was added 3,3-dimethylacryloylchloride (1.96 mL, 0.017 mol) under N2 at 0° C. The mixture was slowly warmed to RT and stirred for 12 h. The reaction was quenched by the addition of H2O (20.0 mL), the organic layer was separated, dried over Na2SO4 and evaporated to dryness to yield crude compound which was used without purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08247430B2 |
| 出典データセット | uspto-grants-2012_08 |
| ORD ID | ord-075960414edf481099c04b6dcf2897ff |
| 出典メモ | uspto-grants-2012_08 |