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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958443Generated: November 1, 2026

Acetic Anhydride → HCID 178504702, compound

https://huagongshe.com/reaction/1958443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Amino-3-[4-(methanesulfonyl)phenyl]-1,2-oxazole-5-carboxamideHCID 57496379—
SolventEthyl orthoformateHCID 31214—
ProductHCID 178504702HCID 178504702—

Reaction Steps

To a suspension of 4-amino-3-(4-methanesulfonyl-phenyl)-isoxazole-5-carboxylic acid amide (2.5 g, 8.9 mmol) in CH(OEt)3 (30 mL), was added acetic anhydride (10 mL) at ambient temperature. The reaction was heated to reflux for 5 h and cooled to room temperature. The reaction was concentrated under vacuum and poured into H2O (50 mL). The organic material was extracted with ethyl acetate (50 mL), dried over MgSO4 and concentrated under vacuum. The crude product was used for the next step without further purification. LCMS 292.0 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410119B2
Source datasetuspto-grants-2013_04
ORD IDord-29b4a0050fe241adaa40e54a6c277b19
Source noteuspto-grants-2013_04