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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571283Generated: October 31, 2026

Methanesulfonyl chloride → HCID 86681691, compound

https://huagongshe.com/reaction/571283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 28491724HCID 28491724—
SolventPyridineHCID 1049—
ProductHCID 86681691HCID 86681691108.6%

Reaction Steps

To a solution of methyl 2-(5-amino-1,3-dioxoisoindolin-2-yl)acetate (380 mg, 1.622 mmol) in pyridine (10 ml), methanesulfonyl chloride (190 μl, 2.434 mmol) was added, and the mixture was reacted overnight at room temperature. The solvent was evaporated and the resulting crude was partitioned between 1N HCl (10 ml) and EtOAc (10 ml); aqueous phase was extracted with EtOAc (3×20 ml) and the organic phase was dried over sodium sulfate. The solvent was removed affording title compound as a brown solid (550 mg, MS/ESI+ 312.9 [MH]+). It was used in the next step without any additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-0e2a9bf1ba574ac79e16a8fe4625bdb6
Source noteuspto-grants-2015_05