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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662622Generated: October 29, 2026

2,5-Bis(2,2,2-trifluoroethoxy)benzene-1-sulfonyl chloride → (2S)-1-[1-{[2,5-bis (2,2,2-trifluoroethoxy)phenyl]sulfonyl}-5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-in dol-3-yl]-N,N-dimethylpiperidine-2-carboxamide

https://huagongshe.com/reaction/1662622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Bis(2,2,2-trifluoroethoxy)benzene-1-sulfonyl chlorideHCID 2736077—
Reactant(2S)-1-[5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-N,N-dimethylpiperidine-2-carboxamideHCID 67429052—
Product(2S)-1-[1-{[2,5-bis (2,2,2-trifluoroethoxy)phenyl]sulfonyl}-5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-in dol-3-yl]-N,N-dimethylpiperidine-2-carboxamideHCID 5986789966.6%

Reaction Steps

With 200 mg of (2S)-1-[5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-N,N-dimethylpiperidine-2-carboxamide, which is the compound described in Preparation 3.49 (Isomer B) of the brochure No. WO01/98295, and 183 mg of 2,5-bis(2,2,2-trifluoroethoxy)benzene sulfonyl chloride as starting materials, 238 mg of the title compound (colorless amorphous) was obtained by a similar method to Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-059cc39c6919452f9040f369017eb268
Source noteuspto-grants-2011_10