HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(2-Nitrophenyl)-1,3,4-oxadiazol-2-amine → 5-(2-Aminophenyl)-1,3,4-oxadiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(2-Nitrophenyl)-1,3,4-oxadiazol-2-amine | HCID 712042 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Product | 5-(2-Aminophenyl)-1,3,4-oxadiazol-2-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138414B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-d726a4112522467aa7270fe17a87f474 |
| Source note | uspto-grants-2006_11 |