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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592996Generated: October 31, 2026

N-(1-benzylpiperidin-4-yl)-2-nitro-4-methylsulphonylaniline → N-(1-benzylpiperidin-4-yl)-2-amino-4-methylsulphonylaniline

https://huagongshe.com/reaction/1592996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-benzylpiperidin-4-yl)-2-nitro-4-methylsulphonylanilineHCID 9281505—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-(1-benzylpiperidin-4-yl)-2-amino-4-methylsulphonylanilineHCID 6870467284.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

The crude material from step 1 (170 g) was dissolved in 3 litres of methanol in a pressure vessel, 20 g of moist 5% Pd/C catalyst was added and stirred under an atmosphere of hydrogen at 3 bar and 50° C. for one hour. The reaction was cooled, filtered and evaporated to give 133 g N-(1-benzylpiperidin-4-yl)-2-amino-4-methylsulphonylaniline as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294636B2
Source datasetuspto-grants-2007_11
ORD IDord-cc1fcd5e26f745c7890f5317bdfd005f
Source noteuspto-grants-2007_11