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Hydrazine → N-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrazine | HCID 9321 | — |
| 反応物 | Hydrazine, propyl- | HCID 42007 | — |
| 反応物 | 5-Methoxy-1,3,4-thiadiazol-2-yl isocyanate | HCID 45123466 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamide | HCID 21454627 | — |
反応手順
A solution of propylhydrazine (0.3 mole) in methylene chloride (150 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 5-Methoxy-1,3,4-thiadiazol-2-yl isocyanate dimer (0.1 mole) is then added, with stirring, at room temperature. After the addition is completed the reaction mixture is heated at reflux for a period of about 4 hours. After this time the reaction mixture is stripped of solvent and excess hydrazine to yield the desired product 2-propyl-4-(5-methoxy-1,3,4-thiadiazol-2-yl)semicarbazide as the residue.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04007031 |
| 出典データセット | uspto-grants-1977_02 |
| ORD ID | ord-5278aac87e224c37aed868ec31f8f32f |
| 出典メモ | uspto-grants-1977_02 |