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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931701Generated: November 2, 2026

Ethyl Acetate → HCID 57965018, compound

https://huagongshe.com/reaction/1931701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-2-methoxypyridineHCID 11622335—
ReactantTert-butyl 4-(4-chloro-1H-pyrazolo[3,4-D]pyrimidin-1-YL)piperidine-1-carboxylateHCID 57964905—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 57965018HCID 5796501854%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 4-(4-chloro-pyrazolo[3,4-d]pyrimidin-1-yl)-piperidine-1-carboxylic acid tert-butyl ester (Intermediate 19; 50 mg, 0.15 mmol), 5-hydroxy-2-methoxypyridine (Tyger Scientific, Ewing, N.J., USA; 24 mg, 0.19 mmol), and potassium carbonate (27 mg, 0.19 mmol) in dimethylformamide (2 mL) was heated in the microwave oven at 160° C. for 10 min. Ethyl acetate and water were added, and the aqueous layer was extracted twice with ethyl acetate. The ethyl acetate layers were combined, evaporated, and purified by preparative C18 HPLC, eluting with 10-100% acetonitrile/water. Samples containing the product were extracted twice with dichloromethane and the solvent was evaporated to give 4-[4-(6-methoxy-pyridin-3-yloxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (34 mg, 54%) as a white powder. Mass spectrum (ES) MH+=427. HRMS Calcd. for C21H27N6O4 (MH+): 427.2089. Found: 427.2088.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188098B2
Source datasetuspto-grants-2012_05
ORD IDord-bb94d7e56cbd4cbbae26db74c9b63e6d
Source noteuspto-grants-2012_05