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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574218Generated: November 1, 2026

Trichloroisocyanuric Acid → HCID 71515812, compound

https://huagongshe.com/reaction/574218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroisocyanuric AcidHCID 6909—
ReactantHCID 71515758HCID 71515758—
SolventAcetonitrileHCID 6342—
ProductHCID 71515812HCID 71515812—

Reaction Steps

To (R)-2-(5-(3-amino-6-methoxy-5-(trifluoromethyl)pyridin-2-yl)-1,3,4-oxadiazol-2-yl)-1,1,1-trifluoropropan-2-ol (Example 2) (150 mg, 0.403 mmol) in acetonitrile (1 ml) was added trichloroisocyanuric acid (37.5 mg, 0.161 mmol) and the resulting mixture was heated using microwave radiation at 100° C. for 30 minutes followed by 125° C. for 10 minutes. The mixture was partitioned between EtOAc and water. The organic portion was separated and washed with sat.NaHCO3, brine, dried (MgSO4) and concentrated in vacuo. Purification of the crude product by chromatography on silica eluting with 0-30% EtOAc in iso-hexane afforded the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034879B2
Source datasetuspto-grants-2015_05
ORD IDord-f8d8375556f64031ba7f70d1f844aa0b
Source noteuspto-grants-2015_05