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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

반응식

참여 물질

역할이름HCID투입량
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
반응물5-Methyl-2-furohydrazideHCID 4159250—
반응물4-[(2,3-Dichloro-4-fluorophenyl)carbonyl]-2-piperazinoneHCID 66599335—
용매DichloromethaneHCID 6344—
생성물7-[(2,3-Dichloro-4-fluorophenyl)carbonyl]-3-(5-methyl-2-furanyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501946B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-933b32bdb9e4402083144a41a3e74732
출처 메모uspto-grants-2013_08