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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852482Generated: November 1, 2026

Potassium tert-butoxide → HCID 178499450, compound

https://huagongshe.com/reaction/1852482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-butyl 4-(4-carbamoyl-3-{[4-(2-methoxy-2-oxoethyl)phenyl]amino}-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylateHCID 86729389—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 178499450HCID 178499450—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-Butyl 4-(4-carbamoyl-3-{[4-(2-methoxy-2-oxoethyl)phenyl]amino}-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylate (226 mg, 0.46 mmol) in THF (2.3 mL) at 0° C. was added KOtBu (0.68 mL, 0.68 mmol, 1.0M in THF), and the mixture was stirred at 0° C. for 20 minutes, then ambient temperature for 20 minutes. The mixture was diluted with saturated aqueous NH4Cl, and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. Et2O (5 mL) was added to the resulting oily residue and a solid precipitated out. This solid was collected by decant, and washed with Et2O to afford the title compound. LRMS (ESI) calc'd for C13H15N4O3 [M+H]+: 275. Found: 275.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962608B2
Source datasetuspto-grants-2015_02
ORD IDord-8ed422a1a7504791a16650a0c06fc589
Source noteuspto-grants-2015_02