HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-formyl-2-phenylacetamide → 5-benzyl-1-(2,3-dichlorophenyl)-1H-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-formyl-2-phenylacetamide | HCID 3268658 | — |
| Reactant | 2,3-Dichlorophenylhydrazine HCl | HCID 12276572 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-benzyl-1-(2,3-dichlorophenyl)-1H-1,2,4-triazole | HCID 16678904 | — |
Reaction Steps
N-Formylphenylacetamide (Finkbeiner J. Org. Chem. 1965, 30; 2861) (200 mg, 1.22 mmol) and 2,3-dichlorophenylhydrazine hydrochloride (314 mg, 1.47 mmol) were combined in glacial acetic acid (8 mL) and refluxed under a nitrogen atmosphere for 1 hour and then concentrated under reduced pressure at 60° C. The residue was purified by flash chromatography eluting with hexanes/ethyl acetate (6/1) to provide the title compound. MS (ESI+) m/z 305 (M+1H)+; 1H NMR (300 MHz, DMSO-d6) δ ppm 4.02 (s, 2H) 6.97-7.02 (m, 2H) 7.16-7.25 (m, 3H) 7.52-7.58 (m, 2H) 7.88 (dd, J=6.8, 3.1 Hz, 1H) 8.16 9s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709469B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-59258f021c294dd98808f01ec494dca2 |
| Source note | uspto-grants-2010_05 |