HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-nitro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Nitroindole | HCID 22523 | — |
| Reactant | 4-Piperidone hydrochloride | HCID 3084851 | — |
| Product | 5-nitro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole | HCID 53263 | — |
Reaction Steps
Using the procedure of Example 1, a mixture of 0.8 g of 5-nitro-1H-indole, 1.53 g of the hydrate of 4-piperidone hydrochloride and 16 ml of 2 N methanolic potassium hydroxide was reacted to obtain 0.86 g of raw product which was crystallized from isopropanol to obtain 0.74 g of 5-nitro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole melting at 250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232031 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-d8e074239ac74d2b92ae90c148763121 |
| Source note | uspto-grants-1980_11 |