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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1641453생성일: 2026년 10월 27일

Phosphorus oxybromide → pentyl 3-bromo-1-(3-chloro-2-pyridinyl)-4,5-dihydro-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1641453

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxybromideHCID 24613—
반응물Sodium BicarbonateHCID 516892—
반응물Pentyl 2-(3-chloro-2-pyridinyl)-5-oxopyrazolidine-3-carboxylateHCID 59549450—
용매AcetonitrileHCID 6342—
생성물pentyl 3-bromo-1-(3-chloro-2-pyridinyl)-4,5-dihydro-1H-pyrazole-5-carboxylateHCID 59549455137.5%

반응 단계

A mixed solution comprising 1.2 g of pentyl 2-(3-chloropyridin-2-yl)-5-oxopyrazolidine-3-carboxylate, 0.59 g of phosphorus oxybromide and 18 ml of acetonitrile was gradually heated, and 25 minutes later, the mixed solution was refluxed with heating for one hour. After the reaction liquid was stood to cool, it was slowly added to a saturated sodium hydrogen carbonate aqueous solution, followed by stirring for 5 minutes. The mixed liquid was subjected to extraction with ethyl acetate, and the organic layer was washed with a sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 to 8/2) to obtain 1.06 g of the desired product (melting point: 39 to 42° C.) in the form of pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08115006B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-b47c9ea67e0f4747a6b5cd6689948e58
출처 메모uspto-grants-2012_02