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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802827Generated: November 1, 2026

Acetic Acid → 5-Chloro-7-nitro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-1H-indole

https://huagongshe.com/reaction/1802827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperazin-2-oneHCID 231360—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Chloro-3-formyl-7-nitro-2-phenyl-1H-indoleHCID 86643834—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Chloro-7-nitro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-1H-indoleHCID 6847636486.1%

Reaction Steps

5-Chloro-3-formyl-7-nitro-2-phenyl-1H-indole (0.5 g, 1.66 mmol) obtained in Step 1 was dissolved in dichloromethane (20 mL), and thereto acetic acid (0.10 g, 1.66 mmol), 2-oxopiperazine (0.3 g, 3.32 mmol) and sodium triacetoxy borohydride (0.71 g, 3.32 mmol) were added in drops. The mixture was stirred at room temperature for 4 hours. At the end of reaction, the mixture was diluted with water, and extracted with dichloromethane. The extract was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and filtered. The solvent was removed under reduced pressure and the residue was separated by column chromatography to give 5-chloro-7-nitro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-1H-indole (0.55 g, Yield 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349885B2
Source datasetuspto-grants-2013_01
ORD IDord-7d6ff5c4580a42dc995ae346e28f01d0
Source noteuspto-grants-2013_01