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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028421Generated: October 30, 2026

Water → 2-[1-Benzyl-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]-N-methylethane-1-sulfonamide

https://huagongshe.com/reaction/1028421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Methyl-4-piperidoneHCID 74049—
Reactant2-(1-Benzyl-1H-indol-5-yl)-N-methylethane-1-sulfonamideHCID 66973924—
SolventMethanolHCID 887—
Product2-[1-Benzyl-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]-N-methylethane-1-sulfonamideHCID 29983971—

Reaction Conditions

Temperature62.5 °C

Reaction Steps

2-(1-benzyl-1H-indol-5-yl)-ethanesulfonic acid methylamide (100 g) was dissolved in methanol (1000 ml) and N-methyl-4-piperidone (100 ml) was added thereto at 25° C. The reaction mass was stirred for 15 minutes and potassium hydroxide (200 g) was added at 25° C. The reaction mass was heated to 60-65° C. for 8 hours and cooled gradually to 25° C. Water (2500 ml) was added slowly and stirred the mixture till solid is obtained. The solid was filtered and dried at 50-55° C. under vacuum to obtain the title compound (Yield: 98 g, HPLC Purity: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735589B2
Source datasetuspto-grants-2014_05
ORD IDord-c142dc2283a4497eb649aa6d9f0cf864
Source noteuspto-grants-2014_05