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Ethyl Acetate → 5-Nitro-2-(1-pyrrolidinyl)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-Nitro-2-(1-pyrrolidinyl)pyridine | HCID 316823 | — |
反応手順
To a stirring mixture of 2-chloro-5-nitropyridine (5.0 g, 31.5 mmol), potassium carbonate (7.0 g, 50.4 mmol), in 65 ml of DMF add pyrrolidine (6.7 g, 95 mmol) and stir at room temperature for 72 h. Dilute reaction mixture with 100 ml EtOAc and wash 2 times with 100 ml saturated NaHCO3, and 2 times with 100 ml of brine. Dry organics over Na2SO4, and evaporate in vacuo to obtain 5-nitro-2-pyrrolidin-1-yl-pyridine. Mass spec.: m+1=194 (AP+). B. 6-Pyrrolidin-1-yl-pyridin-3-ylamine
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06943199B2 |
| 出典データセット | uspto-grants-2005_09 |
| ORD ID | ord-5c7010abf7794b8eba450c893c6f2590 |
| 出典メモ | uspto-grants-2005_09 |