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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190769Generated: October 30, 2026

Acetic Anhydride → HCID 66879643, compound

https://huagongshe.com/reaction/2190769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(3-Aminopyridin-4-yl)-5-(trifluoromethyl)benzoxazoleHCID 66880168—
SolventWaterHCID 962—
ProductHCID 66879643HCID 66879643—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 0.28 g of 2-(3-aminopyridin-4-yl)-5-(trifluoromethyl)benzoxazole and 3 ml of acetic anhydride was stirred while heating at 60° C. for two hours. The reaction mixture was cooled to room temperature, and then water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was washed with ethyl acetate to give 0.17 g of N-[4-(5-trifluoromethylbenzoxazole-2-yl)pyridin-3-yl]acetamide (hereinafter, referred to as “active compound 82”).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324387B2
Source datasetuspto-grants-2012_12
ORD IDord-24e5d2cd55eb4bcd8c81dcccfe5f9163
Source noteuspto-grants-2012_12