HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethoxy)benzoyl chloride → HCID 45140730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethoxy)benzoyl chloride | HCID 522854 | — |
| Reactant | HCID 45140344 | HCID 45140344 | — |
| Product | HCID 45140730 | HCID 45140730 | 57% |
Reaction Steps
Method H was used with 4-(5-amino-2,3,4-trifluorophenoxy)-3-nitropyridin-2-amine and 3-(trifluoromethoxy)benzoyl chloride to afford the title compound (140 mg, 57%). 1H NMR δ (DMSO): 6.26 (d, 1H, Hpy,5, J=5.5 Hz), 7.35 (s, 2H, NH2), 7.55 (t, 1H, Harom,6′, J=6.5 Hz), 7.66 (d, 1H, Harom), 7.71 (t, 1H, Harom,5″, J=8.0 Hz), 7.91 (s, 1H, Harom,2″), 8.00 (d, 1H, Harom), 8.08 (d, 1H, HPy,6, J=5.5 Hz), 10.63 (s, 1H, NHamide). 19F NMR δ (DMSO): −56.28 (s, 3F, CF3), −141.42 (d, 1F, aromF, J=21.5 Hz), −152.31 (d, 1F, aromF, J=21.5 Hz), −156.04 (t, 1F, F3, J=21.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951819B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-f572a2a880324054aee8e83bae6c7639 |
| Source note | uspto-grants-2011_05 |