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3,5-Diamino-1,2,4-triazole → HCID 178509286、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,5-Diamino-1,2,4-triazole | HCID 15078 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 4-[3-(1-Piperidinylmethyl)phenoxy]butanal | HCID 21297547 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 178509286 | HCID 178509286 | 36.3% |
反応手順
A solution of 4-[3-(1-piperidinylmethyl)phenoxy]butanal (522 mg) and 3,5-diamino-1,2,4-triazole (200 mg) in absolute ethanol (20 ml) was heated under reflux for 2 h. The cooled solution was treated with sodium borohydride (200 mg) and stirred at room temperature for 18 hr. The mixture was evaporated in vacuo and the residue partitioned between ethyl acetate and water. The combined organic extracts were evaporated in vacuo and the residue was chromatographed on silica with methanol as eluant to give the title compound as an oil (250 mg), TLC silica (ethyl acetate:isopropanol:water:ammonia 25:15:8:2) 0.4, NMR (CDCl3) 2.8 t (1H); 3.0-3.3 m (3H); 5.3 m (2H); 6.2 m (2H); 6.6-6.8 m (4H); 7.7 m (4H); 8.0-8.8 m (10H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04318913 |
| 出典データセット | uspto-grants-1982_03 |
| ORD ID | ord-c1ab0e48a8f741f493bda1ccc1800c3c |
| 出典メモ | uspto-grants-1982_03 |