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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174552Generated: October 30, 2026

Thionyl Chloride → HCID 68352149, compound

https://huagongshe.com/reaction/2174552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant[4-(methoxycarbonyl)-1H-pyrazol-1-yl]acetic acidHCID 19576734—
ReactantHCID 68352047HCID 68352047—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 68352149HCID 6835214997.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2-(4-(methoxycarbonyl)-1H-pyrazol-1-yl)acetic acid (ChemCollect GmbH, 401 mg, 2.175 mmol) in toluene (10 mL) was added thionyl chloride (0.317 mL, 4.35 mmol) and the reaction mixture was stirred at 90° C. for 2 h. The solvent was removed under reduced pressure and the residue was added to a solution of methyl 4-amino-6-chloro-4′-(piperidin-1-yl)-[1,1′-biphenyl]-3-carboxylate (Intermediate 48) (500 mg, 1.45 mmol) in dichloromethane (10 mL). The reaction mixture was stirred at room temperature overnight. Solvent was removed under reduced pressure and water was added. Precipitate was observed, solid was filtered and dried to give the title compound methyl 1-(2-((2-chloro-5-(methoxycarbonyl)-4′-(piperidin-1-yl)-[1,1′-biphenyl]-4-yl)amino)-2-oxoethyl)-1H-pyrazole-4-carboxylate (720 mg, 1.409 mmol, 97% yield) as a cream solid. LCMS: (M+H)+=511; Rt=4.04 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061998B2
Source datasetuspto-grants-2015_06
ORD IDord-273341e8e9454b4a842a380b9b47784c
Source noteuspto-grants-2015_06