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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964973Generated: November 1, 2026

Carbonic Acid → 2,4-difluoro-3-[hydroxy-(5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methyl]-phenol

https://huagongshe.com/reaction/1964973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonic AcidHCID 767—
ReactantPotassium HydroxideHCID 14797—
Reactant5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridineHCID 51358551—
ReactantCarbonic acid tert-butyl ester 2,4-difluoro-3-formyl-phenyl esterHCID 58086191—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2,4-difluoro-3-[hydroxy-(5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methyl]-phenolHCID 58086212—

Reaction Steps

To carbonic acid tort-butyl ester 2,4-difluoro-3-formyl-phenyl ester (39, 0.405 g, 15.7 mmol) in methanol (36 mL), under an atmosphere of nitrogen, was added 5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridine (89, 288.0 mg, 14.8 mmol, prepared as in Example 17, Scheme 32) and potassium hydroxide (145.0 mg, 25.9 mol). The reaction was stirred at room temperature overnight. The reaction was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The desired compound was isolated by silica gel column chromatography eluting with 4% methanol in methylene chloride to give a colorless oil (P-0009, 0.23 g, 44.1%). MS(ESI) [M+H+]+=354.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415469B2
Source datasetuspto-grants-2013_04
ORD IDord-74fbb786d6684ee08528a3853536b9f2
Source noteuspto-grants-2013_04