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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528346Generated: November 4, 2026

Trifluoroacetic acid → HCID 89443621, compound

https://huagongshe.com/reaction/1528346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 140660332HCID 140660332—
SolventDichloromethaneHCID 6344—
ProductHCID 89443621HCID 8944362163.8%

Reaction Steps

A solution of tert-butyl (2-cyclohexylethyl){6-[({[(Z)-(4-methyl-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate (100 mg, 0.187 mmol, 1 eq.) in dichloromethane (5 ml) was treated with trifluoroacetic acid (0.144 mL, 1.867 mmol, 10 eq.) and refluxed overnight. The reaction was quenched by addition of NaHCO3 sat. aq. and extracted with EtOAc (3×20 ml). The organics were combined, washed with aq. sat. NaCl, dried over MgSO4 and concentrated. After concentration, the residue was purified by chromatography on silica gel to give 3-[(Z)-[({6-[(2-cyclohexylethyl)amino]pyridin-2-yl}methoxy)imino](phenyl)methyl]-4-methyl-1,2,4-oxadiazol-5(4H)-one (52 mg, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090600B2
Source datasetuspto-grants-2015_07
ORD IDord-e2805dd8dc0740928a6fb3ece702cb7d
Source noteuspto-grants-2015_07