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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891136Generated: October 26, 2026

2-Pyridinesulfonamide,5-chloro-(8CI,9CI) → 5-chloro-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}-2-pyridinesulfonamide

https://huagongshe.com/reaction/891136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyridinesulfonamide,5-chloro-(8CI,9CI)HCID 22244571—
ReactantPhenyl 2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamateHCID 22244671—
Product5-chloro-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}-2-pyridinesulfonamideHCID 22244686—

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 5-chloro-2-pyridinesulfonamide: MS (ESI) m/z 564 [M+H]+, 562 [M−H]−, 1H-NMR (CDCl3) δ 78.54 (1H, s), 7.96-7.90 (2H, m), 7.47-7.19 (7H, m), 6.91-6.79 (2H, m), 6.65 (1H, br.s) 5.98 (1H, br.s), 3.44 (2H, t, J=6.6 Hz), 2.83 (2H, t, J=6.7 Hz), 2.20 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001917B2
Source datasetuspto-grants-2006_02
ORD IDord-3eec3cc24b2c47da8d54ed1b95b6b8ca
Source noteuspto-grants-2006_02