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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891134Generated: October 27, 2026

2,4-Dimethylthiazole-5-sulfonamide → 2,4-dimethyl-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}-1,3-thiazole-5-sulfonamide

https://huagongshe.com/reaction/891134

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethylthiazole-5-sulfonamideHCID 12873188—
ReactantPhenyl 2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethylcarbamateHCID 22244671—
Product2,4-dimethyl-N-{[(2-{4-[5-methyl-4-phenyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]phenyl}ethyl)amino]carbonyl}-1,3-thiazole-5-sulfonamideHCID 22244683—

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 2,4-dimethyl-1,3-thiazole-5-sulfonamide: MS (ESI) m/z 564 [M+H]+, 562 [M−H]−, 1H-NMR (CDCl3) δ 7.45-7.32 (9H, m), 6.19 (1H, br.s), 3.49 (2H, t, J=6.6 Hz), 2.89 (2H, t, J=6.6 Hz), 2.67 (3H, s), 2.60 (3H, s), 2.21 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001917B2
Source datasetuspto-grants-2006_02
ORD IDord-8517903016564160a00275340cb75768
Source noteuspto-grants-2006_02