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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641453Generated: October 25, 2026

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

https://huagongshe.com/reaction/1641453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
ReactantSodium BicarbonateHCID 516892—
ReactantPentyl 2-(3-chloro-2-pyridinyl)-5-oxopyrazolidine-3-carboxylateHCID 59549450—
SolventAcetonitrileHCID 6342—
Productpentyl 3-bromo-1-(3-chloro-2-pyridinyl)-4,5-dihydro-1H-pyrazole-5-carboxylateHCID 59549455137.5%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115006B2
Source datasetuspto-grants-2012_02
ORD IDord-b47c9ea67e0f4747a6b5cd6689948e58
Source noteuspto-grants-2012_02