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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571209Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86681621, compound

https://huagongshe.com/reaction/571209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1094646-15-7HCID 43165394—
SolventPyridineHCID 1049—
ProductHCID 86681621HCID 86681621—

Reaction Steps

To a solution of methyl 2-(5-amino-1H-indol-1-yl)acetate (730 mg, 3.54 mmol) in pyridine (15 ml), methanesulfonyl chloride (418 μl, 5.36 mmol) was added, and the mixture was reacted for 2 hours at room temperature. The solvent was evaporated and the resulting crude was partitioned between 1N HCl and ethyl acetate; the aqueous phase was extracted with ethyl acetate (3×30 ml) and dried over sodium sulfate. The solvent was removed obtaining crude methyl 2-(5-(methylsulfonamido)-1H-indol-1-yl)acetate that was used in the next step without any additional purification (1 g, 3.54 mmol, quantitative yield). MS/ESI+ 283.3 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-1fa3df13da0c4a9d9a6176260c0ccabf
Source noteuspto-grants-2015_05