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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521234Generated: October 30, 2026

2-Propanol, 1-methoxy-2-methyl- → 2-Methoxy-1,1-dimethylethyl 4-{4-carbamoyl-3-[(4-fluorophenyl)amino]-1H-pyrazol-1-yl}-4-(cyanomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/521234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Propanol, 1-methoxy-2-methyl-HCID 77137—
ReactantTriphosgeneHCID 94429—
Reactant4-(4-carbamoyl-3-((4-fluorophenyl)amino)-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidin-1-ium 2,2,2-trifluoroacetateHCID 86729401—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-1,1-dimethylethyl 4-{4-carbamoyl-3-[(4-fluorophenyl)amino]-1H-pyrazol-1-yl}-4-(cyanomethyl)piperidine-1-carboxylateHCID 86729407—

Reaction Steps

A solution of 1-methoxy-2-methyl-2-propanol (91 mg, 0.88 mmol) in THF (1.5 mL) and TEA (0.20 mL, 1.4 mmol) was cooled to 0° C. and allowed to stir. Triphosgene (260 mg, 0.876 mmol) was added and the resulting mixture was allowed to warm to ambient temperature and was stirred for 15 minutes. A solution of 4-{4-carbamoyl-3-[(4-fluorophenyl)amino]-1H-pyrazol-1-yl}-4-(cyanomethyl)piperidinium trifluoroacetate (Intermediate #38-5) (80 mg, 0.18 mmol) and TEA (0.061 mL, 0.44 mmol) in DCM (1.0 mL) was then added to the reaction mixture dropwise. The resulting mixture was heated to 50° C. and allowed to stir for 16 hours. The solution was cooled to ambient temperature, diluted with DCM, washed with water, dried over anhydrous MgSO4, and concentrated in vacuo. The resulting residue was purified by MPLC on silica gel (using a gradient elution of 0-10% MeOH/DCM) to afford the title compound, Example #28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-5c26ebc64f024e9f95d70d7e3c383e21
Source noteuspto-grants-2016_05