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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537866Generated: October 26, 2026

4-(2-Chlorooxazol-5-yl)benzonitrile → HCID 178509592, compound

https://huagongshe.com/reaction/537866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Chlorooxazol-5-yl)benzonitrileHCID 68443558—
ReactantHCID 178507542HCID 178507542—
SolventIsopropanolHCID 3776—
ProductHCID 178509592HCID 178509592100.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(2-chlorooxazol-5-yl)benzonitrile 2 (0.216 g, 1.05 mmol) and commercially available 3-(1H-tetrazol-5-yl)aniline 35 (0.17 g, 1.05 mmol) in 2-propanol (20 mL) was heated to 80° C. for 18 h with stirring. Upon cooling, a white solid precipitated out which was filtered off, washed with 2-propanol, and dried. This was further purified by dissolving into DMSO and re-precipitated with addition of water. Resulting solid was filtered, washed with water, methanol and dried under high vacuum to yield 4-(2-((3-(1H-tetrazol-5-yl)phenyl)amino)oxazol-5-yl)benzonitrile 36 as a white solid (0.348 g, 100%). MS (ES) m/z 330 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865709B2
Source datasetuspto-grants-2014_10
ORD IDord-1c09c89417e34647ab4c1efe2db7dede
Source noteuspto-grants-2014_10