HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Anisoyl chloride → HCID 58024296, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Anisoyl chloride | HCID 74374 | — |
| Reactant | 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one | HCID 45140141 | — |
| Product | HCID 58024296 | HCID 58024296 | 40% |
Reaction Steps
Method H was used with 7-(3-aminophenoxy)-1H-imidazo[4,5-b]pyridin-2(3H)-one and 3-methoxy-benzoyl chloride to afford the title compound as a brown solid (21 mg, 40%). 1H-NMR (δ, ppm, DMSO-d6): 3.83 (s, 3H, OMe), 6.49 (d, 1H, HPy,5, J=5.8 Hz), 6.90 (d, 1H, Harom, J=7.48 Hz), 7.16 (d, 1H, Harom, J=6.52 Hz), 7.39-7.49 (m, 3H, Harom), 7.52 (d, 1H, Harom, J=7.61 Hz), 7.62-7.68 (m, 2H, Harom), 7.81 (d, 1H, HPy,6, J=5.44 Hz), 10.31 (s, 1H, NHamide), 11.19 (s, 1H, NHPy3), 11.39 (s, 1H, NHPy2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951819B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-d4814be2465d4e648aa476cb94f7931e |
| Source note | uspto-grants-2011_05 |