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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288369Generated: November 1, 2026

4-Methylamino-3-nitrobenzenesulfonic acid-n-methyl-n-(1-methylpiperidin-4-yl)amide → HCID 18412481, compound

https://huagongshe.com/reaction/2288369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylamino-3-nitrobenzenesulfonic acid-n-methyl-n-(1-methylpiperidin-4-yl)amideHCID 18412661—
ReactantDichloromethane ethanolHCID 21584144—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
ProductHCID 18412481HCID 18412481—

Reaction Steps

1.5 g (4.4 mMol) of 4-methylamino-3-nitrobenzenesulphonic acid-N-methyl-N-(1-methyl-piperidin-4-yl)-amide were dissolved in 100 ml methanol and catalytically hydrogenated at room temperature and under 5 bar hydrogen pressure (10% palladium on charcoal). Then the catalyst was filtered off and the filtrate was evaporated down. The resulting oily product was further reacted without any purification. Yield: 1.4 g (100% of theory), C14H24N4O2S (312.4) Rf value: 0.33 (silica gel; dichloromethane/ethanol=4:1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06087380
Source datasetuspto-grants-2000_07
ORD IDord-4d88d9efcd6442f48189eb3fed9ca4d7
Source noteuspto-grants-2000_07