HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenyl-1H-pyrazole-5-carbonyl chloride → HCID 45142204, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenyl-1H-pyrazole-5-carbonyl chloride | HCID 2776565 | — |
| Reactant | 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one | HCID 45140141 | — |
| Product | HCID 45142204 | HCID 45142204 | 17% |
Reaction Steps
Method H was used with 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one and 1-phenyl-1H-pyrazole-5-carbonyl chloride to afford the title compound (15 mg, 17%). 1H-NMR (δ, ppm, DMSO-d6): 6.47 (d, 1H, HPy,5, J=6.0 Hz), 6.89 (d, 1H, Harom, J=8.0 Hz), 7.06 (d, 1H, Hpyrrazole, J=2.1 Hz), 7.37-7.49 (m, 7H, Harom), 7.53 (d, 1H, Harom, J=8.0 Hz), 7.78-7.81 (m, 2H, Hpyrrazole+Py,6), 10.64 (s, 1H, NHamide), 11.16 (s, 1H, NHPy3), 11.37 (s, 1H, NHPy2). HRMS (EI): m/z [M+H] calcd for C22H17N6O3: 413.1362; found: 413.1366.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951819B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-8a85618aca524b5d8f2aebf1e00b951e |
| Source note | uspto-grants-2011_05 |