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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367357Generated: October 28, 2026

5-Nitroindole → 3-(1,2,3,4,5,8-Hexahydroindolizin-7-yl)-5-nitro-1H-indole

https://huagongshe.com/reaction/367357

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitroindoleHCID 22523—
ReactantOctahydroindolizin-7-oneHCID 11240524—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
Product3-(1,2,3,4,5,8-Hexahydroindolizin-7-yl)-5-nitro-1H-indoleHCID 1538976038.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133290
Source datasetuspto-grants-2000_10
ORD IDord-2451b33206af4f8e8e64568122ae9596
Source noteuspto-grants-2000_10