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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891130Generated: October 30, 2026

2,4-Difluorobenzenesulfonamide → 3-[1-(4-{2-[({[(2,4-Difluorophenyl)sulfonyl]amino}carbonyl)amino]ethyl}phenyl)-3,5-dimethyl-1H-pyrazol-4-yl]benzamide

https://huagongshe.com/reaction/891130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DifluorobenzenesulfonamideHCID 574964—
Reactantphenyl 2-(4-{4-[3-(aminocarbonyl)phenyl]-3,5-dimethyl-1H-pyrazol-1-yl}phenyl)ethylcarbamateHCID 22244565—
Product3-[1-(4-{2-[({[(2,4-Difluorophenyl)sulfonyl]amino}carbonyl)amino]ethyl}phenyl)-3,5-dimethyl-1H-pyrazol-4-yl]benzamideHCID 22244668—

Reaction Steps

The title compound was prepared according to the procedure described in step 1 of Example 42 from phenyl 2-(4-{4-[3-(aminocarbonyl)phenyl]-3,5-dimethyl-1H-pyrazol-1-yl}phenyl)ethylcarbamate (step 6 of example 72) and 2,4-difluorobenzensulfonamide: MS (ESI) m/z 554 [M+H]+, 552 [M−H]−, 1H-NMR (CDCl3) δ 8.00-7.98 (1H, m), 7.83-7.73 (3H, m), 7.56-7.44 (2H, m), 7.22 (4H, s), 7.05-6.94 (1H, m), 6.20 (1H, br.s), 5.66 (1H, br.s), 3.47 (2H, t, J=6.2 Hz), 2.85 (2H, t, J=6.2 Hz), 2.21 (3H, s), 2.20 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001917B2
Source datasetuspto-grants-2006_02
ORD IDord-5ab8beeca5c847d088a3e041baf66788
Source noteuspto-grants-2006_02