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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456422생성일: 2026년 10월 26일

Diisopropylethylamine → (R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazine

https://huagongshe.com/reaction/456422

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Tetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
반응물(R)-Octahydro-pyrido[1,2-a]pyrazineHCID 773775—
반응물Pyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]-HCID 12449554—
용매Dimethyl SulfoxideHCID 679—
용매DichloromethaneHCID 6344—
생성물(R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazineHCID 2079906398.1%

반응 조건

온도160 °C

반응 단계

A mixture of the dihydrochloride salt of (R)-octahydropyrido[1,2-a]pyrazine (649 mg, 3.05 mmol), diisopropylethylamine (1.17 ml, 6.72 mmol), 3-chloro-6-(4-trifluoromethylphenyl)-pyridazine (290 mg, 1.12 mmol) and dimethylsulfoxide (1 ml) was heated in a closed vessel at 160° C. for 40 min. The reaction mixture was cooled to room temperature, diluted with dichloromethane (10 ml) and washed with water (2×15 ml) and brine (15 ml). The organic layer was dried over magnesium sulphate. The solvent was removed in vacuo to give 398 mg of the title compound as the free base.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186721B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-bfd189a0842d47fd8b77df7eb5d727b1
출처 메모uspto-grants-2007_03