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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427136Generated: October 31, 2026

Methanol → 3-[[2-(4-Hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-2,4-dimethyl-benzoic acid

https://huagongshe.com/reaction/1427136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-[[2-(4-hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-2,4-dimethyl-benzoateHCID 86707369—
SolventTetrahydrofuranHCID 8028—
Product3-[[2-(4-Hydroxy-1-piperidyl)quinoline-4-carbonyl]amino]-2,4-dimethyl-benzoic acidHCID 8670737031.1%

Reaction Steps

A solution of aqueous 2N NaOH (2.00 ml) is added to a stirred solution of methyl 3-(2-(4-hydroxypiperidin-1-yl)quinoline-4-carboxamido)-2,4-dimethylbenzoate (0.10 g, 0.00023 mol) in THF:MeOH (4 ml:2 ml). After 5 h at 50° C., the organic solvent is removed under reduced pressure and the residue is diluted with water, acidified to pH 6 with aqueous 1N HCl, and extracted with ethyl acetate (2×20 ml). The organic layers are combined and dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure and the resulting precipitate is triturated with pentane and diethyl ether and filtered to afford the title compound as a light yellow solid (0.03 g, 31%). Mass spectrum (m/z): 420.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933098B2
Source datasetuspto-grants-2015_01
ORD IDord-d8de3b2434034cdfabe9bdad39ce190a
Source noteuspto-grants-2015_01