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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676534Generated: October 26, 2026

3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide → 4-amino-3-isopropoxy-N-(1-methyl-piperidin-4-yl)-benzamide

https://huagongshe.com/reaction/1676534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamideHCID 67076401—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-amino-3-isopropoxy-N-(1-methyl-piperidin-4-yl)-benzamideHCID 5801499995.3%

Reaction Steps

To a solution of 1.2 g (3.6 mmole) of 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide in 25 mL of methanol was added 0.12 g of 10% palladium on carbon. The hydrogenation reaction was carried out under 50 psi of hydrogen for 2 hours. The mixture was filtered, concentrated under reduced pressure and triturated with ether. The solid was collected by filtration, washed with ether and dried under vacuum to give 1.0 g of 4-amino-3-isopropoxy-N-(1-methyl-piperidin-4-yl)-benzamide as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003785B2
Source datasetuspto-grants-2011_08
ORD IDord-695d0ef61d084dc6ab4ef81caf607ec8
Source noteuspto-grants-2011_08