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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521239Generated: October 29, 2026

Propionyl chloride → 1-[4-(Cyanomethyl)-1-propanoylpiperidin-4-yl]-3-(phenylamino)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/521239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionyl chlorideHCID 62324—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[4-Carbamoyl-3-(phenylamino)-1H-pyrazol-1-yl]-4-(cyanomethyl)piperidinium trifluoroacetateHCID 86729383—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(Cyanomethyl)-1-propanoylpiperidin-4-yl]-3-(phenylamino)-1H-pyrazole-4-carboxamideHCID 86729414—

Reaction Steps

To a suspension of 4-[4-carbamoyl-3-(phenylamino)-1H-pyrazol-1-yl]-4-(cyanomethyl)piperidinium trifluoroacetate (Intermediate #38-1) (50 mg, 0.11 mmol) in THF (1 mL) was added DIPEA (0.060 mL, 0.34 mmol), followed by propanoyl chloride (0.020 mL, 0.18 mmol). The resulting mixture was allowed to stir for 18 hours before the reaction mixture was concentrated in vacuo to afford an orange oil. The residue was dissolved in DMSO (2 mL) and purified by mass-triggered reverse phase preparative HPLC (MeCN/water, with 0.1% v/v TFA modifier). Desired fractions were identified, combined, diluted with saturated aqueous NaHCO3 and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo to afford the title compound, Example #33-1, as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-0466931882984dba9c29ae4e3fd53335
Source noteuspto-grants-2016_05