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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351658Generated: November 2, 2026

Water → 1-((2-Fluorophenyl)methyl)pyrazolo(3,4-b)pyridine-3-carbonitrile

https://huagongshe.com/reaction/351658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxamideHCID 11323178—
SolventTetrahydrofuranHCID 8028—
Product1-((2-Fluorophenyl)methyl)pyrazolo(3,4-b)pyridine-3-carbonitrileHCID 11402500—

Reaction Conditions

Temperature40 °C

Reaction Steps

36.1 g (133 mmol) of 1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxamide from Example 22A are dissolved in 330 ml of THF and mixed with 27 g (341 mmol) of pyridine. Over a period of 10 min, 47.76 ml (71.66 g, 341 mmol) of trifluoroacetic anhydride are subsequently added, and the temperature increases to 40° C. during the addition. The mixture is stirred at room temperature overnight. The mixture is subsequently poured into 1 l of water, and the mixture is extracted three times with 0.5 l of ethyl acetate each time. The organic phase is washed with saturated sodium bicarbonate solution and with 1 N HCl, dried with MgSO4 and concentrated using a rotary evaporator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743798B1
Source datasetuspto-grants-2004_06
ORD IDord-5ea9c129f4964750a5b66b4feecba39c
Source noteuspto-grants-2004_06