化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 6,7-Dichloro-4-ethyl-3,4-dihydro-2H-pyrazino(2,3-b)(1,4)oxazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Tetrachloropyrazine | HCID 311820 | — |
| 反応物 | Oxazine | HCID 12313776 | — |
| 反応物 | Ethylaminoethanol | HCID 18179409 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 6,7-Dichloro-4-ethyl-3,4-dihydro-2H-pyrazino(2,3-b)(1,4)oxazine | HCID 21429939 | 12% |
反応手順
Tetrachloropyrazine (22 g, 0.1 mol), ethylaminoethanol (9 g, 0.1 mol), and crushed KOH (16.5 g, 85% assay, 0.25 mol) were contacted overnight in 200 ml of refluxing benzene. Work-up gave a mixture of the oxazine (25%) and of the O-adduct (75%). The mixture was dissolved in THF and triethylamine (20 g, 0.2 mol) was added and held at reflux temperature for 6 days. The solid was filtered, the THF rotary evaporated, and the residual oil was partitioned between water and CH2Cl2. The organic layer was dried (MgSO4) and rotary evaporated to leave an oily residue. This was recrystallized from hexane and IPA to give two crops totaling 2.8 g (12% yield), m.p. 108°-10°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04029657 |
| 出典データセット | uspto-grants-1977_06 |
| ORD ID | ord-35cd28cf629c4e9284f7530a8a2b9bbb |
| 出典メモ | uspto-grants-1977_06 |