HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (E)-N-Methyl-2-[3-(4-hydroxy-1-methyl-4-piperidinyl)-1H-indol-5-yl]ethenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Methyl-4-piperidone | HCID 74049 | — |
| Reactant | 2-(1H-indol-5-yl)-N-methylethenesulfonamide | HCID 13475764 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (E)-N-Methyl-2-[3-(4-hydroxy-1-methyl-4-piperidinyl)-1H-indol-5-yl]ethenesulphonamide | HCID 19068423 | 64% |
Reaction Steps
A mixture of (E)-N-methyl-2-(1H-indole-5-yl)ethenesulphonamide (2.0 g), 1-methyl-4-piperidone (1.62 g) and potassium hydroxide (0.7 g) in IMS (20 mL) was stirred at ambient temperature for 22 hr. The reaction mixture was concentrated and the residue purified by column chromatography on silica gel. Eluting with dichloromethane/ethanol/ammonia (25:10:1) gave an oil which solidified on standing to a brown solid. Trituration with ether provided the product as a white powder (1.85 g, 64% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05659040 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-a98f55042771491cb8e73dff09c3e775 |
| Source note | uspto-grants-1997_08 |