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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41170Generated: October 25, 2026

Hydrochloric Acid → 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid

https://huagongshe.com/reaction/41170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylateHCID 86672406—
SolventMethanolHCID 887—
Product8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic acidHCID 8667240235.8%

Reaction Conditions

Temperature40 °C

Reaction Steps

An aqueous NaOH 2N (0.622 mL, 1.24 mmol) solution was added to methyl 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate (195 mg, 0.41 mmol) in MeOH (2 mL) and the reaction mixture stirred at 40° C. for 6 h. The mixture was cooled to 0° C. and an aqueous HCl 2N (0.684 mL, 1.37 mmol) solution was added dropwise to the reaction mixture until pH ˜5. The solution was partially concentrated and a precipitate appeared. Water was added to the slurry and extracted with DCM. The organic phase was washed with water, dried over MgSO4, filtered and concentrated. The formed precipitate was triturated with ether, filtered, washed with ether, dried under vacuum at 50° C. to afford 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid (67 mg, 35%) as a pale beige solid. Mass Spectrum: m/z [M+H]+=457.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530470B2
Source datasetuspto-grants-2013_09
ORD IDord-8b838650d64b461fa655d81b1cb228f7
Source noteuspto-grants-2013_09