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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12185Generated: October 26, 2026

6-chloro-7-(4-methyl-piperazin-1-yl)-8-nitro-9H-beta-carboline → 6-chloro-7-(4-methyl-piperazin-1-yl)-8-amino-9H-beta-carboline

https://huagongshe.com/reaction/12185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-chloro-7-(4-methyl-piperazin-1-yl)-8-nitro-9H-beta-carbolineHCID 67165626—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-chloro-7-(4-methyl-piperazin-1-yl)-8-amino-9H-beta-carbolineHCID 6716673755.2%

Reaction Steps

Suspended 236 mg of 6-chloro-7-(4-methyl-piperazin-1-yl)-8-nitro-9H-β-carboline in 100 ml of methanol and added 10% Pd/C(48 mg) under argon. The flask was flushed with hydrogen (3×) and the reaction mixture was stirred under a hydrogen atmosphere at RT overnight. The reaction mixture was filtered and Pd/C was removed using a pad of celite. The reaction mixture was evaporated to remove solvent and purified by flash chromatography to give 119 mg (55% yield) of the desired 6-chloro-7-(4-methyl-piperazin-1-yl)-8-amino-9H-β-carboline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727985B2
Source datasetuspto-grants-2010_06
ORD IDord-999c390fd09a4602b272acf153fb1264
Source noteuspto-grants-2010_06