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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1889079생성일: 2026년 10월 24일

Triethyloxonium tetrafluoroborate → HCID 66598910, 화합물

https://huagongshe.com/ko/reaction/1889079

반응식

참여 물질

역할이름HCID투입량
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
반응물5-FluoropicolinohydrazideHCID 55280967—
반응물4-[(2,4-Dichloro-3-fluorophenyl)carbonyl]-2-piperazinoneHCID 66599361—
용매DichloromethaneHCID 6344—
생성물HCID 66598910HCID 66598910—

반응 단계

To a solution of 4-[(2,4-dichloro-3-fluorophenyl)carbonyl]-2-piperazinone (I37) (0.146 g, 0.5 mmol) in Dichloromethane (DCM) (3 mL) was added triethyloxonium tetrafluoroborate (0.100 g, 0.525 mmol). The solution was then stirred, under argon, for 10 minutes before 5-fluoro-2-pyridinecarbohydrazide (I24) (0.093 g, 0.600 mmol) was added. The solution was then stirred for a further hour before the solvent was concentrated and n-butanol (3.00 mL) was added. The solution was then stirred, under argon and reflux, for 3 hours before being cooled to room temperature. The solvent was then evaporated in vacuo and the remaining residue was purified by flash chromatography (Biotage SP4, 25M cartridge) with a gradient of 0-10% 2M NH3/MeOH in DCM. TLC confirmed product location and the solvent from the combined fractions was evaporated in vacuo. The remaining residue was then further purified by mass-direct automated HPLC, and the solvent evaporated in vacuo. The remaining solid was then triturated with ether and dried in a vac-oven to yield the product in 0.045 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501946B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-825fc682cea94cc295592bac89d03ba1
출처 메모uspto-grants-2013_08