Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1889089생성일: 2026년 10월 25일
Triethyloxonium tetrafluoroborate → 7-[(2,3-Dichloro-4-fluorophenyl)carbonyl]-3-(5-methyl-2-furanyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine
https://huagongshe.com/reaction/1889089
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 반응물 | 5-Methyl-2-furohydrazide | HCID 4159250 | — |
| 반응물 | 4-[(2,3-Dichloro-4-fluorophenyl)carbonyl]-2-piperazinone | HCID 66599335 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 7-[(2,3-Dichloro-4-fluorophenyl)carbonyl]-3-(5-methyl-2-furanyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine | HCID 66599074 | — |
반응 단계
Triethyloxonium tetrafluoroborate (197 mg, 1.039 mmol) was added to a solution of the 4-[(2,3-dichloro-4-fluorophenyl)carbonyl]-2-piperazinone (I34) (275 mg, 0.945 mmol) in Dichloromethane (DCM) (6 mL) and the reaction was stirred for 1 h. To this was added the 5-methyl-2-furancarbohydrazide (I85) (159 mg, 1.134 mmol) and the reaction was stirred for 2 h. The solvent was evaporated and 1-butanol (6.00 mL) was added. The mixture was heated at reflux for 3 h. LCMS: Product peak observed. After cooling the solvent was evaporated and the residue was partitioned between water/EtOAc. The organic layer was dried (Na2SO4) and the solvent evaporated to afford a brown oil. This was purified by MDAP to afford a colourless solid of desired material in 38 mg.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08501946B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-933b32bdb9e4402083144a41a3e74732 |
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| 출처 메모 | uspto-grants-2013_08 |
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