Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332389Generated: October 25, 2026

Sodium Hydroxide → 6-[(5-Methyl-3-phenyl-isoxazol-4-ylmethyl)-amino]-nicotinic acid

https://huagongshe.com/reaction/332389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinateHCID 68443539—
SolventEthanolHCID 702—
Product6-[(5-Methyl-3-phenyl-isoxazol-4-ylmethyl)-amino]-nicotinic acidHCID 6844640191.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 6-[(5-methyl-3-phenyl-isoxazol-4-ylmethyl)-amino]-nicotinic acid methyl ester (1.86 g, 5.50 mmol) in ethanol (100 mL) was added aqueous sodium hydroxide (1 N, 17 mL, 17 mmol) and the resulting suspension was heated to 80° C. for 0.5 h. After the solution was cooled to ambient temperature the solvent was distilled off and the residue was diluted with water (50 mL) and washed with tert-butylmethylether (50 mL). The organic layers were extracted with aqueous sodium hydroxide (1 N, 20 mL) and the combined aqueous layers were acified with aqueous hydrochloric acid (25%) to pH=3 and were extracted with a mixture of ethyl acetate and methanol (4:1, 30 mL). Drying over sodium sulfate and concentration afforded the title compound (1.55 g, 91%) which was obtained as a white solid. MS: m/e=310.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877783B2
Source datasetuspto-grants-2014_11
ORD IDord-f5d65c52c2d145f8bb6a553f1fe12ceb
Source noteuspto-grants-2014_11