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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891120Generated: October 25, 2026

2-Fluorobenzenesulfonamide → 2-Fluoro-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamide

https://huagongshe.com/reaction/891120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorobenzenesulfonamideHCID 193663—
ReactantPhenyl 2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamateHCID 22244671—
Product2-Fluoro-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}benzenesulfonamideHCID 11713669—

Reaction Steps

The title compound was prepared according to the procedure described in step 1 of Example 42 from phenyl 2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamate (step 7 of Example 52) and 2-fluoro-benzenesulfonamide: MS (ESI) m/z 547 [M+H]+, 545 [M−H]−, 1H-NMR (CDCl3) δ 7.86-7.81 (1H, m), 7.74-7.58 (1H, m), 7.48-7.24 (1H, m), 6.45 (1H, br.s) 3.54-3.49 (2H, m), 2.87 (2H, t, J=6.7 Hz), 2.23 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001917B2
Source datasetuspto-grants-2006_02
ORD IDord-3863af43450c4862a88f6d4e9fa24c05
Source noteuspto-grants-2006_02