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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13325Generated: October 27, 2026

Trifluoroacetic acid → N-(4-benzyloxy-5-fluoro-2-nitrophenyl)pyrazinecarboxamide

https://huagongshe.com/reaction/13325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium NitrateHCID 24434—
ReactantN-(4-benzyloxy-3-fluorophenyl)pyrazinecarboxamideHCID 23145734—
SolventChloroformHCID 6212—
ProductN-(4-benzyloxy-5-fluoro-2-nitrophenyl)pyrazinecarboxamideHCID 23145743—

Reaction Steps

40 ml of trifluoroacetic acid and 1.99 g of potassium nitrate were added to a chloroform (40 ml) suspension of 5.80 g of N-(4-benzyloxy-3-fluorophenyl)pyrazinecarboxamide, with cooling with ice, and the reaction liquid was stirred overnight at room temperature. The solvent was evaporated away under reduced pressure, and aqueous saturated sodium bicarbonate was added to it. The resulting solid was washed with a mixed solvent of ethyl acetate and hexane to obtain the entitled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-ca3065c4765142768db3178da2f15c3d
Source noteuspto-grants-2010_06