HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 121679-21-8
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Methyl-4-piperidone | HCID 74049 | — |
| Reactant | 2-(1H-Indol-5-yl)-N-methylethane-1-sulfonamide | HCID 13475765 | — |
| Product | 121679-21-8 | HCID 20066733 | — |
Reaction Steps
A solution of N-methyl-1H-indole-5-ethanesulphonamide (1.0 g) in methanol (50 ml) containing potassium hydroxide (5.6 g) and N-methyl-4-piperidone (1.0 ml) was heated at reflux for 24h, cooled, and the resulting solid filtered off (1.0 g). A sample of the solid (0.2 g) was dissolved in a hot methanolic solution of oxalic acid (0.06 g), the solution cooled, and the salt precipitated by adding ethyl acetate (20 ml) and dry ether (50 ml). The salt was filtered off, and dried in vacuo to give the title compound as a solid (0.12 g) m.p. 87°-90° (shrinks) Analysis Found: C,52.2; H,5.6; N,9.5. C17H23N3O2S.C2H2O4.0.6H2O requires C,52.5; H,6.0; N,9.7%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04997841 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-36c743241eb8401dbd961db09df5d8c6 |
| Source note | uspto-grants-1991_03 |