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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250556Generated: October 26, 2026

Water → (3-dibenzylamino-2,6-difluoro-phenyl)-(5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanol

https://huagongshe.com/reaction/250556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridineHCID 51358551—
Reactant3-Dibenzylamino-2,6-difluoro-benzaldehydeHCID 58087884—
SolventMethanolHCID 887—
Product(3-dibenzylamino-2,6-difluoro-phenyl)-(5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanolHCID 58087074—

Reaction Steps

To 3-dibenzylamino-2,6-difluoro-benzaldehyde (53, 0.76 g, 2.3 mmol) in methanol (50 mL) were added 5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridine (89, 0.40 g, 2.1 mmol, prepared as described in Example 17) and potassium hydroxide (0.50 g, 8.9 mmol) under an atmosphere of nitrogen. 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 filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 5% methanol in methylene chloride to provide the compound (54, 0.60 g, 50%). MS (ESI) [M+H+]+=533.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863288B2
Source datasetuspto-grants-2011_01
ORD IDord-4360fc6ae85b45588e9767fdad78e9af
Source noteuspto-grants-2011_01