HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Trifluoromethylnicotinoyl chloride → ethyl N-(4-trifluoromethyl-nicotinoyl)-2-chlorobenzimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Trifluoromethylnicotinoyl chloride | HCID 11790465 | — |
| Reactant | Ethyl 2-chlorobenzimidate | HCID 13092607 | — |
| Product | ethyl N-(4-trifluoromethyl-nicotinoyl)-2-chlorobenzimidate | HCID 21283736 | — |
Reaction Steps
starting from ethyl o-chlorobenzimidate and 4-trifluoromethyl-nicotinoyl chloride there is obtained ethyl N-(4-trifluoromethyl-nicotinoyl)-2-chlorobenzimidate and therefrom with methylhydrazine there is obtained 3-(o-chlorophenyl)-1-methyl-5-(4-trifluoromethyl-3-pyridyl)-1H-1,2,4-triazole, 1H-NMR(CDCl3): 3.85 (s, N-CH3), 7.6-8.1 (5 aromatic H), 8.9-9.2 (2 aromatic H); mass spectrum: 338 (100), 319 (5), 166 (94), 138 (95);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788210 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-2101eefffada49e7b64f0037a4dcda9b |
| Source note | uspto-grants-1988_11 |