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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258652Generated: October 25, 2026

Tetrahydrofuran → 5-Chloro-2-methylamino-4-(4-trifluoromethyl-piperidin-1-yl)aniline

https://huagongshe.com/reaction/1258652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chloro-N-methyl-2-nitro-5-(4-trifluoromethyl-piperidin-1-yl)anilineHCID 44120655—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product5-Chloro-2-methylamino-4-(4-trifluoromethyl-piperidin-1-yl)anilineHCID 67958171—

Reaction Steps

A mixture of 4-chloro-N-methyl-2-nitro-5-(4-trifluoromethyl-piperidin-1-yl)aniline (1.07 g, 3.2 mmol), THF (20 mL), MeOH (30 mL) and Pt/C (100 mg) was stirred for 6 h at rt under a hydrogen atmosphere (3 bar). The catalyst was removed by filtration and the mixture was concentrated to give the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466186B2
Source datasetuspto-grants-2013_06
ORD IDord-32e54dccf7194f78a479279bb11def23
Source noteuspto-grants-2013_06