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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662591Generated: October 30, 2026

2,5-Bis(2,2,2-trifluoroethoxy)benzene-1-sulfonyl chloride → (4R)-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]-4-hydroxy-N,N-dimethyl-L-prolinamide

https://huagongshe.com/reaction/1662591

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Bis(2,2,2-trifluoroethoxy)benzene-1-sulfonyl chlorideHCID 2736077—
Reactant(2S,4R)-1-(5-Chloro-3-(2-methoxyphenyl)-2-oxoindolin-3-YL)-4-hydroxy-N,N-dimethylpyrrolidine-2-carboxamideHCID 67044068—
Product(4R)-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]-4-hydroxy-N,N-dimethyl-L-prolinamideHCID 5986794966.8%

Reaction Steps

With 100 mg of (4R)-1-[5-chloro-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-L-prolinamide (levorotatory isomer), which is the compound described in Preparation 3.2 (Isomer B) of the brochure Publication No. WO01/55130, and 89 mg of 2,5-bis (2,2,2-trifluoroethoxy)benzene sulfonyl chloride as starting materials, 119 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-8348b5f92fa34fa1a6279c94037de063
Source noteuspto-grants-2011_10