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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581910Generated: October 25, 2026

4-Oxazolin-2-one → HCID 178511990, compound

https://huagongshe.com/reaction/1581910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Oxazolin-2-oneHCID 186114—
Reactant4-ethoxymethylene-2-(1)-naphthyl-5(4H)-oxazoloneHCID 356930—
ReactantHCID 178511989HCID 178511989—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178511990HCID 178511990—

Reaction Steps

4-(2-Naphthalen-1-yl-5-oxo-oxazol-4-ylidenemethyl)-N-phenyl-piperazine-1-carboxamidine was prepared as described in commonly owned U.S. patent applications U.S. S.No. 60/124,781; filed on Mar. 17, 1999; U.S. S.No. 60/165,312, filed on Nov. 12, 1999; and U.S. Ser. No. 09/521,185, filed Mar. 8, 2000 by Coffen, et al. entitled “Oxazolone Derivatives and Uses Thereof”, filed herewith. Briefly, to a 0.25 M solution of N-phenyl-piperazine-1-carboxamidine (200 μL, 50 μmole) was added a 0.25 M solution of 4-ethoxymethylene-2-naphthalene-1-yl-4H-oxazol-5-one in DMSO (200 μL, 25 μmole). The reaction vessel was sealed and the resulting mixture shaken at room temperature for 1 h to yield the desired product as a DMSO solution (MH+426).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06733982B1
Source datasetuspto-grants-2004_05
ORD IDord-6457fcbfcb904f77915d8ebc439fdeb8
Source noteuspto-grants-2004_05