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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Methyl-4-piperidone | HCID 74049 | — |
| Reactant | 2-(1-Benzyl-1H-indol-5-yl)-N-methylethane-1-sulfonamide | HCID 66973924 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-[1-Benzyl-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indol-5-yl]-N-methylethane-1-sulfonamide | HCID 29983971 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735589B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-c142dc2283a4497eb649aa6d9f0cf864 |
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| Source note | uspto-grants-2014_05 |
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