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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261546Generated: November 3, 2026

Water → (1H-Pyrrolo[2,3-b]pyridin-3-yl)-[6-(4-trifluoromethyl-benzylamino)-pyridin-3-yl]-methanol

https://huagongshe.com/reaction/2261546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant(1H-Pyrrolo[2,3-b]pyridin-3-yl)-[6-(4-trifluoromethyl-benzylamino)-pyridin-3-yl]-methanoneHCID 11632642—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Product(1H-Pyrrolo[2,3-b]pyridin-3-yl)-[6-(4-trifluoromethyl-benzylamino)-pyridin-3-yl]-methanolHCID 5758806730%

Reaction Steps

Into a round bottom flask was added (1H-Pyrrolo[2,3-b]pyridin-3-yl)-[6-(4-trifluoromethyl-benzylamino)-pyridin-3-yl]-methanone P-0017 (210.0 mg, 0.53 mmol) and sodium tetrahydroborate (80.0 mg, 2.11 mmol), dissolved in N,N-dimethylformamide (5.0 mL) and ethanol (20.0 mL). The reaction was stirred at room temperature overnight, poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, concentrated and purified with biotage (dichloromethane/methanol 1:20) to give compound 14 (63 mg, yield=30%) as a white solid. MS (ESI) [M+H+]+=399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846941B2
Source datasetuspto-grants-2010_12
ORD IDord-a9e941be7be24420a93a692dc0874e92
Source noteuspto-grants-2010_12