HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(6-Acetyl-2-chloro-3-methoxyphenyl)-4-cyclobutylthiazole-2-carboxamide → HCID 178487690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(6-Acetyl-2-chloro-3-methoxyphenyl)-4-cyclobutylthiazole-2-carboxamide | HCID 66730303 | — |
| Reactant | HCID 178487691 | HCID 178487691 | — |
| Product | HCID 178487690 | HCID 178487690 | 84% |
Reaction Steps
8-Chloro-7-methoxy-2-(4-cyclobutylthiazol-2-yl)quinolin-4-ol 269b was synthesized from compound 268b (5.68 g, 1 eq.) as a beige solid in 84% yield, following the procedure as described for compound 218a (80° C. overnight). 1H NMR (DMSO-d6, 400 MHz): δ (ppm) 1.87-1.95 (m, 1H), 1.96-2.07 (m, 1H), 2.23-2.35 (m, 4H), 3.67-3.76 (m, 1H), 4.02 (s, 3H), 7.51 (s, 1H), 7.53 (d, J=9.30 Hz, 1H), 7.63 (s, 1H), 8.11 (d, J=9.30 Hz, 1H), 11.89 (br s, 1H); MS (ESI, EI+): m/z=347 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377962B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-d44880ca45d84133abaef69ad8eacfda |
| Source note | uspto-grants-2013_02 |