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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713535Generated: November 2, 2026

Sodium Hydroxide → HCID 23122089, compound

https://huagongshe.com/reaction/1713535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68421596HCID 68421596—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23122089HCID 2312208984.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl N-[(tetrahydro-3-oxo-1,1-diphenyl-3H-oxazolo[3,4-a]pyrazin-7(1H)-yl)carbonyl]glycine (1.5 g, 3.6 mmol) was dissolved in ethanol (10 mL) and tetrahydrofuran (2 mL). With ice cooling, a 4 M aqueous sodium hydroxide solution (1.0 mL, 4.0 mmol) was added thereto, and the mixture was stirred at 0° C. for 3 hours. The reaction solution was concentrated under reduced pressure, and diethyl ether and water were added to the residue. The aqueous layer was neutralized with 4 M hydrochloric acid, which was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and hexane was added to the residue. The resulting mixture was powdered and dried to obtain the title compound (1.2 g, yield 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795267B2
Source datasetuspto-grants-2010_09
ORD IDord-73db9fd5614d4ab3989ed4ae8c10b5db
Source noteuspto-grants-2010_09