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HRID 437028作成日:2026年10月27日

Triethylamine → 6,7-Dichloro-4-ethyl-3,4-dihydro-2H-pyrazino(2,3-b)(1,4)oxazine

https://huagongshe.com/reaction/437028

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Potassium HydroxideHCID 14797—
反応物TetrachloropyrazineHCID 311820—
反応物OxazineHCID 12313776—
反応物EthylaminoethanolHCID 18179409—
溶媒BenzeneHCID 241—
溶媒TetrahydrofuranHCID 8028—
生成物6,7-Dichloro-4-ethyl-3,4-dihydro-2H-pyrazino(2,3-b)(1,4)oxazineHCID 2142993912%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04029657
出典データセットuspto-grants-1977_06
ORD IDord-35cd28cf629c4e9284f7530a8a2b9bbb
出典メモuspto-grants-1977_06