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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| 반응물 | (R)-Octahydro-pyrido[1,2-a]pyrazine | HCID 773775 | — |
| 반응물 | Pyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]- | HCID 12449554 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazine | HCID 20799063 | 98.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07186721B2 |
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| 출처 데이터셋 | uspto-grants-2007_03 |
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| ORD ID | ord-bfd189a0842d47fd8b77df7eb5d727b1 |
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| 출처 메모 | uspto-grants-2007_03 |
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