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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029726Generated: November 4, 2026

1-(3-Fluoro-4-pyridinylamino)-5-phenylmethoxy-1H-indole → 1-(3-Fluoro-4-pyridinylamino)-1H-indol-5-ol

https://huagongshe.com/reaction/1029726

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Fluoro-4-pyridinylamino)-5-phenylmethoxy-1H-indoleHCID 19900464—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(3-Fluoro-4-pyridinylamino)-1H-indol-5-olHCID 19900485137.1%

Reaction Steps

In a 500 ml Parr hydrogenation bottle, 10% Pd/C (1.0 g) was suspended in 50 ml ethanol, and to this was added a solution of 1-(3-fluoro-4-pyridinylamino)-5-phenylmethoxy-1H-indole (5.0 g) in 200 ml ethanol. The mixture was shaken at 50° C. under 50 psi hydrogen gas for two hours. After cooling, the mixture was filtered, and the filtrate was concentrated to give an oil (5.0 g) which was eluted on a silica gel column with ethyl acetate/dichloromethane (1:1) via HPLC. The desired fractions were combined and concentrated to give a crystalline solid, 3.5 g, m.p. 70°-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102891
Source datasetuspto-grants-1992_04
ORD IDord-21665ff9206c436493bf5880b3acc1c8
Source noteuspto-grants-1992_04