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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603944Generated: October 30, 2026

Trifluoroacetic acid → 4-{2-[1-Benzhydryl-6-chloro-2-(2-phenylmethanesulfonylamino-ethyl)-1H-indol-3-yl]-ethoxy}-benzoic acid methyl ester

https://huagongshe.com/reaction/603944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactantmethyl 4-formylmethyloxybenzoateHCID 11636984—
ReactantN-[2-(1-Benzhydryl-6-chloro-1H-indol-2-yl)-ethyl]-C-phenylmethanesulfonamideHCID 16115154—
SolventDichloromethaneHCID 6344—
Product4-{2-[1-Benzhydryl-6-chloro-2-(2-phenylmethanesulfonylamino-ethyl)-1H-indol-3-yl]-ethoxy}-benzoic acid methyl esterHCID 1211369935%

Reaction Steps

To N-[2-(1-Benzhydryl-6-chloro-1H-indol-2-yl)-ethyl]-C-phenyl-methanesulfonamide (0.033M, 1 equiv.) in DCM at 0° C. were added 4-(2-oxo-ethoxy)-benzoic acid methyl ester (3.3 equiv.), triethylsilane (6 equiv.), and TFA (5 equiv.). The reaction mixture was stirred at rt for 2d 20 h before aqueous workup. Purification by silica gel chromatography followed by reverse phase HPLC gave 4-{2-[1-Benzhydryl-6-chloro-2-(2-phenylmethanesulfonylamino-ethyl)-1H-indol-3-yl]-ethoxy}-benzoic acid methyl ester in 35% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906548B2
Source datasetuspto-grants-2011_03
ORD IDord-9ca768f1003043afbf5db72a9d295ff9
Source noteuspto-grants-2011_03