HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline 1-oxide → HCID 178505013, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline 1-oxide | HCID 15366 | — |
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Reactant | {4-[(Methanesulfonyl)amino]phenyl}acetic acid | HCID 2773887 | — |
| Reactant | HCID 69057130 | HCID 69057130 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 178505013 | HCID 178505013 | — |
Reaction Steps
The tile compound was synthesized using N-(4-((5-oxo-4,5-dihydro-1H-pyrazol-3-yl)methyl)phenyl)methanesulfonamide and quinoline N-oxide in acetic anhydride according to the procedure described in Example 23. The N-(4-((5-oxo-4,5-dihydro-1H-pyrazol-3-yl)methyl)phenyl)methanesulfonamide was synthesized using 2-(4-(methylsulfonamido)phenyl)acetic acid and Meldrum's acid. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.91 (s, 3H) 4.08 (s, 1H) 4.43 (s, 1H) 7.10 (d, J=3.79 Hz, 2H) 7.24-7.37 (m, 2H) 7.46 (d, J=6.06 Hz, 1H) 7.67-7.77 (m, 2H) 7.82-7.94 (m, 2H) 8.17-8.29 (m, 1H) 9.60 (s, 1H) 11.40 (s, 1H); ESI-MS: m/z calc'd for C20H18N4O3S 394.45. found 395.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07550598B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-6cbacbf74d0b4a50b98d941de77c96fa |
| Source note | uspto-grants-2009_06 |