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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909874Generated: October 31, 2026

N-methyl-2-pyrrolidone → HCID 58306560, compound

https://huagongshe.com/reaction/1909874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium methanesulfinateHCID 2733271—
Reactantmethyl 5-bromo-1H-indole-7-carboxylateHCID 24728848—
CatalystCupric ChlorideHCID 24014—
SolventEthyl AcetateHCID 8857—
ProductHCID 58306560HCID 5830656030.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of methyl 5-bromo-1H-indole-7-carboxylate (300 mg), 1-methyl-2-pyrrolidinone (6 mL), sodium methanesulfinate (600 mg), and copper iodide (I) (1.10 g) was stirred at 150° C. for 17 hours under an argon atmosphere. The reaction mixture was left to be cooled to room temperature, ethyl acetate was added thereto, and then the insoluble materials were removed by filtration. To this filtrate was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine in this order, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain methyl 5-(methanesulfonyl)-1H-indole-7-carboxylate (91 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598355B2
Source datasetuspto-grants-2013_12
ORD IDord-5d448d9886a243eebe5448ae699c7d18
Source noteuspto-grants-2013_12