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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914077Generated: November 2, 2026

2-(Trifluoromethoxy)benzene-1-sulfonyl chloride → 5-(3,4-Dimethoxyphenyl)-4,4-dimethyl-2-(1-{[2-(trifluoromethoxy)phenyl]-sulfonyl}piperidin-4-yl)-2,4-dihydro-3H-pyrazol-3-one

https://huagongshe.com/reaction/1914077

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethoxy)benzene-1-sulfonyl chlorideHCID 2777215—
Reactant5-(3,4-dimethoxyphenyl)-4,4-dimethyl-2-piperidin-4-yl-2,4-dihydro-3H-pyrazol-3-one hydrochlorideHCID 66616406—
Product5-(3,4-Dimethoxyphenyl)-4,4-dimethyl-2-(1-{[2-(trifluoromethoxy)phenyl]-sulfonyl}piperidin-4-yl)-2,4-dihydro-3H-pyrazol-3-oneHCID 46202724—

Reaction Steps

The title compound is prepared analogously as described for GP1 using 5-(3,4-dimethoxyphenyl)-4,4-dimethyl-2-(piperidin-4-yl)-2,4-dihydro-3H-pyrazol-3-one hydrochloride (compound B1*HCl) and 2-(trifluoromethoxy)benzenesulfonyl chloride as starting compounds. The crude product is purified by crystallization from methanol to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609848B2
Source datasetuspto-grants-2013_12
ORD IDord-654a10fdebb94fcbb26f851dd74c0107
Source noteuspto-grants-2013_12