HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzoyl chloride → HCID 45141110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Reactant | 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one | HCID 45140141 | — |
| Product | HCID 45141110 | HCID 45141110 | 61% |
Reaction Steps
Method H was used with 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one and 4-(trifluoromethyl)benzoyl chloride to afford the title compound as a brown solid (33 mg, 61%). 1H-NMR (δ, ppm, DMSO-d6): 6.50 (d, 1H, HPy,5, J=6.0 Hz), 6.93 (d, 1H, Harom, J=7.0 Hz), 7.44 (t, 1H, Harom, J=8.0 Hz), 7.63 (s, 1H, Harom), 7.64-7.68 (m, 1H, Harom), 7.82 (d, 1H, HPy,6, J=6.0 Hz), 7.91 (d, 2H, Harom, J=8.0 Hz), 8.12 (d, 2H, Harom, J=8.0 Hz), 10.55 (s, 1H, NHamide), 11.20 (s, 1H, NHPy3), 11.38 (s, 1H, NHPy2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951819B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-33fcaf716a8042408c3422f91ee12d4e |
| Source note | uspto-grants-2011_05 |