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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453326Generated: October 25, 2026

Trifluoromethylsulfonamide → N-(3-{1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-propionyl)-C,C,C-trifluoro-methanesulfonamide

https://huagongshe.com/reaction/453326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethylsulfonamideHCID 79001—
Reactant3-{1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-propionyl fluorideHCID 86667289—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-(3-{1-[5-Chloro-(4-chloro-benzyloxy)-benzyl]-5-methyl-1H-pyrazol-3-YL}-propionyl)-C,C,C-trifluoro-methanesulfonamideHCID 8666728872%

Reaction Steps

To a solution of acid fluoride 9 (0.14 g, 0.33 mmol) and DMAP 0.161 g (1.3 mmol) in dry DCM, trifluoromethanesulfonamide 0.147 g (0.98 mmol) was added. The mixture was stirred under a nitrogen atmosphere for 16 hours before diluting with EtOAc. The organic phase was washed with 2M HCl, followed by brine, dried over MgSO4 and evaporated to dryness. The crude acyl sulphonamide 10 was purified on silica to yield 0.13 g as a white solid (72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492424B2
Source datasetuspto-grants-2013_07
ORD IDord-e0210d42a02c48f8befebabf8b50faf8
Source noteuspto-grants-2013_07