Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662611Generated: October 30, 2026

(4R)-4-fluoro-1-[3-(2-methoxyphenyl)-2-oxo-5-(trifluoromethoxy)-2,3-dihydro-1H-indol-3-yl]-N,N-dimethyl-L-prolinamide → (4R)-4-fluoro-1-[3-(2-methoxyphenyl)-1-{[4-methoxy-2-(trifluoromethoxy)phenyl]sulfonyl}-2-o xo-5-(trifluoromethoxy)-2,3-dihydro-1H-indol-3-yl]-N,N-dimethyl-L-prolinamide

https://huagongshe.com/reaction/1662611

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4R)-4-fluoro-1-[3-(2-methoxyphenyl)-2-oxo-5-(trifluoromethoxy)-2,3-dihydro-1H-indol-3-yl]-N,N-dimethyl-L-prolinamideHCID 67429458—
Reactant4-Methoxy-2-(trifluoromethoxy)benzene sulfonyl chlorideHCID 86625684—
Product(4R)-4-fluoro-1-[3-(2-methoxyphenyl)-1-{[4-methoxy-2-(trifluoromethoxy)phenyl]sulfonyl}-2-o xo-5-(trifluoromethoxy)-2,3-dihydro-1H-indol-3-yl]-N,N-dimethyl-L-prolinamideHCID 5986783451.7%

Reaction Steps

With 200 mg of the compound obtained in Step 20-1 (Isomer B) and 133 mg of 4-methoxy-2-(trifluoromethoxy)benzene sulfonyl chloride as starting material, 158 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-e744cb03e36142e29246d5d43a16cd15
Source noteuspto-grants-2011_10