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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571236Generated: October 31, 2026

Methanesulfonyl chloride → HCID 86681653, compound

https://huagongshe.com/reaction/571236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 43446487HCID 43446487—
SolventPyridineHCID 1049—
ProductHCID 86681653HCID 8668165382%

Reaction Steps

To a solution of methyl 2-(5-amino-2-oxoindolin-1-yl)acetate (0.120 g, 0.545 mmol) in pyridine (8 ml) cooled to 0° C., methanesulfonyl chloride (0.047 ml, 0.599 mmol) was added, and the mixture was allowed to warm to room temperature and stirred for 1.5 hours. The solvent was removed and the crude was portioned between DCM and 1N HCl. The organic phase was dried over sodium sulfate, and the solvent was removed. The crude was purified by filtration on silica gel cartridge (DCM:MeOH from 99:1 to 97:3) affording methyl 2-(5-(methylsulfonamido)-2-oxoindolin-1-yl)acetate (0.133 g, 0.446 mmol, 82% yield). MS/ESI+ 298.9 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-0591cb7773964d26af0c89cb1a8db796
Source noteuspto-grants-2015_05