Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395898Generated: October 25, 2026

Hydroxylamine → 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid hydroxyamide

https://huagongshe.com/reaction/1395898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 69449552—
SolventWaterHCID 962—
SolventMeOH tetrahydrofuranHCID 21899815—
Product3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid hydroxyamideHCID 2475390250%

Reaction Steps

To a solution of sodium hydroxide (64 mg, 1.6 mmol) and 50% aqueous hydroxylamine (0.65 mL) was added 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (58 mg, 0.2 mmol) dissolved in THF/MeOH (1 mL, 1:1). After stirring 4 hr at room temperature, the solution was diluted with water (4 mL) and the volatile solvents were removed in vacuo. The solution was then neutralized to pH=7-8 with 1N HCl and then subjected to HPLC purification to provide 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid hydroxyamide (32 mg, 50% yield). 1H NMR (400 MHz, DMSO) δ 11.05 (s, 1H), 8.83 (br s, 1H), 7.97 (s, 1H), 7.57 (dd, 1H, J=1.7, 8.6 Hz), 7.41 (d, 1H, J=8.6 Hz) 7.30 (m, 2H), 7.18 (s, 1H), 7.08 (m, 2H), 4.03 (s, 2H), 3.74 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08900565B2
Source datasetuspto-grants-2014_12
ORD IDord-143a18fdbc884efd951bc5a877438654
Source noteuspto-grants-2014_12