돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437028생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/437028

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium HydroxideHCID 14797—
반응물TetrachloropyrazineHCID 311820—
반응물OxazineHCID 12313776—
반응물EthylaminoethanolHCID 18179409—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
생성물6,7-Dichloro-4-ethyl-3,4-dihydro-2H-pyrazino(2,3-b)(1,4)oxazineHCID 2142993912%

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04029657
출처 데이터셋uspto-grants-1977_06
ORD IDord-35cd28cf629c4e9284f7530a8a2b9bbb
출처 메모uspto-grants-1977_06