化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → 5-amino-3-methyl-1-(2-octyl)-1H-pyrazole-4-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Hydrogen Peroxide | HCID 784 | — |
| 反応物 | Octamoxin | HCID 20811 | — |
| 反応物 | (1-Ethoxyethylidene)malononitrile | HCID 79450 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-amino-3-methyl-1-(2-octyl)-1H-pyrazole-4-carboxamide | HCID 59932333 | — |
反応手順
4.72 g (34.66 mmol) of 2-(1-ethoxy-ethylidene)-malononitrile and 5.00 g (34.66 mmol) of (1-methyl-heptyl)-hydrazine are refluxed for 4 hours in 40 ml of methanol. After the solvent has been removed in vacuo, 8.23 g of a red oil are obtained. This is dissolved in 250 ml of ethanol and, after 300 ml of concentrated NH3 solution (25% strength) and 70 ml of hydrogen peroxide solution (30% strength) have been added, the solution is stirred for 65 hours at room temperature. After the non-aqueous solvents have been removed, the mixture is extracted three times with dichloromethane, and the organic phase is dried over sodium sulphate and evaporated on a rotary evaporator. This gives 7.75 g (87%) of a red oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06174884B1 |
| 出典データセット | uspto-grants-2001_01 |
| ORD ID | ord-b6b918c5f1924368946f04e96b64471e |
| 出典メモ | uspto-grants-2001_01 |