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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987638Generated: November 1, 2026

Quinoline 1-oxide → HCID 178505013, compound

https://huagongshe.com/reaction/1987638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoline 1-oxideHCID 15366—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant{4-[(Methanesulfonyl)amino]phenyl}acetic acidHCID 2773887—
ReactantHCID 69057130HCID 69057130—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 178505013HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550598B2
Source datasetuspto-grants-2009_06
ORD IDord-6cbacbf74d0b4a50b98d941de77c96fa
Source noteuspto-grants-2009_06