Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375408Generated: October 29, 2026

Methanol → N-(2-fluoro-4-methoxyphenyl)-4-hydroxy-1H-indole-3-carboxamide

https://huagongshe.com/reaction/375408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 15337623HCID 15337623—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(2-fluoro-4-methoxyphenyl)-4-hydroxy-1H-indole-3-carboxamideHCID 15337630—

Reaction Steps

N-(2-Fluoro-4-methoxyphenyl)-4-benzyloxy-1H-indole-3-carboxamide (1.34 g, 3.4 mmol), prepared using the method above, was slurried with 10% Palladium on Carbon (134 mg) in ethanol (35 mL) in a Parr bottle and placed under a Hydrogen atmosphere (50 psi) for 5 h. Methanol (5 ml) was added and the mixture returned to the Hydrogen atmosphere for an additional 18 h. The solution was filtered through Celite, concentrated in vacuo, and the residue purified by flash chromatography to afford N-(2-fluoro-4-methoxyphenyl)-4-hydroxy-1H-indole-3-carboxamide (Compound 2) as a beige solid; mp 259°-261° C. (d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484944
Source datasetuspto-grants-1996_01
ORD IDord-c92d1f6d36c94a2ebc22d78ed08dd669
Source noteuspto-grants-1996_01