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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722219Generated: October 26, 2026

5-(2-Nitrophenyl)-1,3,4-oxadiazol-2-amine → 5-(2-Aminophenyl)-1,3,4-oxadiazol-2-amine

https://huagongshe.com/reaction/722219

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Nitrophenyl)-1,3,4-oxadiazol-2-amineHCID 712042—
ReactantHCID 178418361HCID 178418361—
Product5-(2-Aminophenyl)-1,3,4-oxadiazol-2-amineHCID 5093885—

Reaction Steps

Hydrogen was introduced at atmospheric pressure into the solution of 350 mg of 5-(2-nitrophenyl)-[1,3,4]oxadiazol-2-ylamine until the theoretical amount had been taken up. After filtering off the catalyst with suction and concentrating the mixture under reduced pressure, the remaining oily residue was purified by column chromatography (solvent: 95:5 dichloromethane/methanol; silica gel).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138414B2
Source datasetuspto-grants-2006_11
ORD IDord-d726a4112522467aa7270fe17a87f474
Source noteuspto-grants-2006_11