化工社化工社 化学情報印刷レポート · 研究参考用
N,N-Dimethyl-1,3-propanediamine → 2-[2-(3-Dimethylaminopropylamino)-5-thiadiazolyl]-1-methyl-5-nitroimidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-(2-Chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole | HCID 21390801 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 2-[2-(3-Dimethylaminopropylamino)-5-thiadiazolyl]-1-methyl-5-nitroimidazole | HCID 21390856 | — |
反応手順
A mixture consisting of 3.8 gm., 0.0155 mole of 2-(2-chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole, prepared as in Example 16 2.5 gm., 0.029 mole of 3-dimethylaminopropylamine, 2.1 gm. 0.025 mole, of sodium bicarbonate and 100 ml. of benzene is refluxed for 22 hours. The reaction mixture is cooled to room temperature, washed with aqueous sodium bicarbonate and sodium chloride solutions. Cooling to 5° C. gives a crystalline precipitate which is collected and recrystallized from benzene to give the pure compound melting at 153°-154° C. More product is obtained from the mother liquors to give an overall yield of 3.0 gm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03991200 |
| 出典データセット | uspto-grants-1976_11 |
| ORD ID | ord-99b246c9bdc8479c9a0236635a3792a8 |
| 出典メモ | uspto-grants-1976_11 |