HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Nitroindole → 3-(1,2,3,4,5,8-Hexahydroindolizin-7-yl)-5-nitro-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Nitroindole | HCID 22523 | — |
| Reactant | Octahydroindolizin-7-one | HCID 11240524 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 3-(1,2,3,4,5,8-Hexahydroindolizin-7-yl)-5-nitro-1H-indole | HCID 15389760 | 38.2% |
Reaction Steps
A mixture of 5-nitro-1H-indole (4.48 g, 27.6 mmol) and and 7-octahydroindolizinone (5.0 g, 35.9 mmol) in methanolic potassium hydroxide (10% potassium hydroxide in 50 mL of methanol) was heated to reflux for 3.5 hours. The reaction was diluted with water and the precipitate was collected by filtration. The filter cake was triturated with hot diethyl ether and filtered. The filter cake was recrystallized from methanol and dried to give 2.99 g of the title compound. (38.5%). Calculated for C16H17N3O2 : Theory: C, 67.83; H, 6.05; N, 14.83. Found: C, 68.07; H, 6.27; N, 14.82.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133290 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-2451b33206af4f8e8e64568122ae9596 |
| Source note | uspto-grants-2000_10 |