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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454676Generated: October 30, 2026

Citric Acid → HCID 58508897, compound

https://huagongshe.com/reaction/454676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 66990165HCID 66990165—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58508897HCID 58508897—

Reaction Conditions

Temperature55 °C

Reaction Steps

Methanol (2.0 mL) and a 4 mol/L aqueous solution of sodium hydroxide (0.19 mL) were added to a dioxane (2.0 mL) solution of the obtained tert-butyl 2-(2-acetoxy-5-(piperidin-1-yl)benzamido)-4-(1-(tert-butoxycarbonyl)-1H-pyrrol-2-yl)benzoate, followed by stirring at 55° C. for 1 hour. The reaction mixture was cooled to room temperature, and then a 4 mol/L aqueous solution of sodium hydroxide (0.077 mL) was added thereto, followed by stirring at 60° C. for 2 hours. The reaction mixture was cooled to room temperature and then adjusted to a pH of 7.8 with a 10% aqueous solution of citric acid, and water and ethyl acetate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 100-91% chloroform/methanol] to obtain 8 mg of 2-(2-hydroxy-5-(piperidin-1-yl)benzamido)-4-(1H-pyrrol-2-yl)benzoic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-2fcccf454f8f4e73ab34ce6a354527eb
Source noteuspto-grants-2013_07