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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931659Generated: October 26, 2026

Sodium Carbonate → 4-[4-(4-Bromo-2-cyano-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1931659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-hydroxybenzonitrileHCID 2757014—
ReactantTert-butyl 4-(4-chloro-1H-pyrazolo[3,4-D]pyrimidin-1-YL)piperidine-1-carboxylateHCID 57964905—
SolventDimethylformamideHCID 6228—
Product4-[4-(4-Bromo-2-cyano-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl esterHCID 5796491530%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 5-bromo-2-hydroxy-benzonitrile (Oakwood Products, Inc., West Columbia, S.C., USA; 18 mg, 0.089 mmol), 4-(4-chloro-pyrazolo[3,4-d]pyrimidin-1-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 19; 30 mg, 0.089 mmol), and potassium carbonate (27 mg, 0.196 mmol) in dimethylformamide (1 mL) was heated in a microwave oven at 160° C. for 10 min. Saturated sodium carbonate solution was added to the reaction mixture, and the mixture was then filtered through a pad of silica gel to remove the precipitate. The silica gel pad was washed with methanol and the solvents were evaporated from the filtrate. The residue was purified by HPLC to give 4-[4-(4-bromo-2-cyano-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (4 mg, 30%) as a white solid. Mass spectrum MH+=499.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188098B2
Source datasetuspto-grants-2012_05
ORD IDord-13c0e1c16ee640e8a7960d34eb4623a0
Source noteuspto-grants-2012_05