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Dimethylcarbamoyl Chloride → 3-(Cyanomethyl)pyridine-2-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| 反応物 | Trimethylsilyl cyanide | HCID 82115 | — |
| 反応物 | 3-(Cyanomethyl)pyridin-1-ium-1-olate | HCID 243167 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-(Cyanomethyl)pyridine-2-carbonitrile | HCID 4672598 | 66% |
反応手順
To a suspension of (1-oxy-pyridin-3-yl)-acetonitrile (10 g, 75 mmol) in anhydrous CH2Cl2 under a nitrogen atmosphere was added trimethylsilylcyanide (10.95 mL, 82 mmol) and dimethylcarbamoylchloride (7.55 mL, 82 mmol). The reaction mixture was stirred at room temperature for 72 hours and then concentrated. EtOAc (100 mL) was added to the residue and the organic phase was washed with 1 M NaOH (150 mL), dried over Na2SO4, filtered and concentrated. The resulting solid was purified by column chromatography (50% EtOAc/hexanes) affording 7.08 g (66%) of a yellow solid: mp 48-51° C.; MS (+) APCI m/z 144 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06465482B2 |
| 出典データセット | uspto-grants-2002_10 |
| ORD ID | ord-cf89a84d4e8e4c04b7d5e82db027f738 |
| 出典メモ | uspto-grants-2002_10 |