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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388209Generated: November 2, 2026

Hydrochloric Acid → [(7-Hydroxy-4-methyl-3-phenyl-isoxazolo[4,5-c]pyridine-6-carbonyl)-amino]-acetic acid

https://huagongshe.com/reaction/2388209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantGlycineHCID 750—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 7-hydroxy-4-methyl-3-phenylisoxazolo[4,5-c]pyridine-6-carboxylateHCID 67530597—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[(7-Hydroxy-4-methyl-3-phenyl-isoxazolo[4,5-c]pyridine-6-carbonyl)-amino]-acetic acidHCID 4263306477.5%

Reaction Steps

Ethyl 7-hydroxy-4-methyl-3-phenylisoxazolo[4,5-c]pyridine-6-carboxylate (41 mg, 0.138 mmol) was dissolved in 5 mL of DMF. Glycine (207 mg, 2.75 mmol) and sodium ethoxide (140 mg, 2.06 mmol) were added and the mixture was refluxed for 2 h. The mixture was cooled to room temperature and diluted with 30 mL of water. Concentrated hydrochloric acid was added dropwise until pH was 3. The aqueous phase was extracted with EtOAc and the combined organic layer was dried over MgSO4 and concentrated to give 35 mg of pale yellow solid. The solid was dissolved in saturated NaHCO3 (10 mL) and washed with hexanes and EtOAc. The aqueous phase was acidified to pH 3 with concentrated HCl and extracted with EtOAc. The organic layer was dried and concentrated to give 15 mg of the title compound. MS: (+) m/z 328.39 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269008B2
Source datasetuspto-grants-2012_09
ORD IDord-7ce78763ac614eae9f0c9c04ffaa3e47
Source noteuspto-grants-2012_09