化工社化工社 化学情報印刷レポート · 研究参考用
Thiophene-2-carbohydrazide → 2-[3-sulfanyl-5-(thiophen-2-yl)-4H-1,2,4-triazol-4-yl]acetic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thiophene-2-carbohydrazide | HCID 73098 | — |
| 反応物 | Methyl 2-isothiocyanatoacetate | HCID 140795 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 2-[3-sulfanyl-5-(thiophen-2-yl)-4H-1,2,4-triazol-4-yl]acetic acid | HCID 4962553 | — |
反応手順
Methyl N-(thioxomethylene)glycinate (2.06 g) and thiophene-2-carbohydrazide (2.57 g) in isopropanol (50 ml) was heated at 70° C. while stirring for 16 h. The mixture was allowed to come to r.t. and the formed precipitate collected and heated at reflux in 1.0 M aqueous NaHCO3 solution for 2 h. After cooling to r.t. and acidification with conc. HCl (aq.) the product was extracted into EA, which was washed with brine and then dried over MgSO4 before concentration to dryness to yield crude title compound which was used directly in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07576077B2 |
| 出典データセット | uspto-grants-2009_08 |
| ORD ID | ord-4cb66b5c39fd4368b8e29fbcc8210ca3 |
| 出典メモ | uspto-grants-2009_08 |