化工社化工社 化学情報印刷レポート · 研究参考用
Acetic Acid → (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 2-Amino-5-bromopyrazine | HCID 599539 | — |
| 反応物 | 1,3-dimethyl-1H-pyrazole-4-carbaldehyde | HCID 847285 | — |
| 反応物 | Borane,N-dimethylmethanamine (1:1) | HCID 6327651 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine | HCID 86614303 | 92.9% |
反応手順
A mixture of 1,3-dimethyl-1H-pyrazole-4-carbaldehyde (142 mg, 1.145 mmol), 2-amino-5-bromopyrazine (200 mg, 1.149 mmol), borane trimethylamine complex (126 mg, 1.73 mmol) and glacial acetic acid (137 mg, 2.29 mmol) in anhydrous methonol (3 ml) was stirred at room temperature overnight. The reaction mixture was then diluted with ethyl acetate, washed with water, dried over MgSO4 and filtered. The filtrate was concentrated to give 300 mg of (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine as crude product, which was used for next step reaction without further purification. Crude yield: 93%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07875622B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-38087498dc564989a3268c1e6140769d |
| 出典メモ | uspto-grants-2011_01 |