HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloronicotinoyl Chloride → 6-Chloro-N-(3,2',4'-trifluoro-biphenyl-4-yl)-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloronicotinoyl Chloride | HCID 2782165 | — |
| Reactant | 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide | HCID 59318138 | — |
| Reactant | 3,2',4'-Trifluoro-biphenyl-4-ylamine | HCID 59318163 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Chloro-N-(3,2',4'-trifluoro-biphenyl-4-yl)-nicotinamide | HCID 59318055 | — |
Reaction Steps
6-Chloro-N-(3,2′,4′-trifluoro-biphenyl-4-yl)-nicotinamide was prepared from 3,2′,4′-trifluoro-biphenyl-4-yl amine and 6-chloronicotinoyl chloride following a procedure similar to the one described in the synthesis of 6-chloro-N-(4-iodo-3-methyl-phenyl)-nicotinamide, above. The product was isolated after a silica gel column chromatography with 0-30% EtOAc in hexanes. H1 NMR (300 MHz, chloroform-d) d ppm 6.91 (m, 2H), 7.15 (apparent t, J=8.1 Hz, 1H), 7.24-7.1 (m, 3H), 7.95 (dd, J=10.5 8.1 Hz, 2H), 8.69 (d, J=2.1 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324385B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-a84197496ab44f699decf74b13cfd7ee |
| Source note | uspto-grants-2012_12 |