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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419615Generated: October 30, 2026

1-[2-Methyl-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperidine → 5-Methyl-2-(methyloxy)-4-{4-[2-(methylsulfonyl)ethyl]-1-piperidinyl}aniline

https://huagongshe.com/reaction/419615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-Methyl-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperidineHCID 59452654—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
Product5-Methyl-2-(methyloxy)-4-{4-[2-(methylsulfonyl)ethyl]-1-piperidinyl}anilineHCID 5945265359.3%

Reaction Steps

To 1-[2-methyl-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperidine (3.26 g, 9.14 mmol) in EtOAc (100 mL) was added platinum on carbon (sulfided) (1.77 g, 0.460 mmol). The mixture was stirred under H2 (1 atm.) overnight. Filtering the mixture through Celite® and concentrating provided the title compound of Step E (1.77 g, 5.42 mmol, 59%). 1H NMR (400 MHz, DMSO-d6) δ 6.55 (s, 1H), 6.43 (s, 1H), 4.29 (s, 2H), 3.71 (s, 3H), 3.10-3.19 (m, 2H), 2.97 (s, 3H), 2.88 (d, 2H), 2.51-2.58 (m, 2H), 2.06 (s, 3H), 1.61-1.79 (m, 4H), 1.19-1.52 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-7ee2202c85324d8399364ca45b82ed04
Source noteuspto-grants-2012_01