Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258628Generated: October 27, 2026

Tetrahydrofuran → 5-Chloro-2-methylamino-4-(3-(trifluoromethyl)piperidin-1-yl)aniline

https://huagongshe.com/reaction/1258628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-chloro-N-methyl-2-nitro-5-(3-(trifluoromethyl)piperidin-1-yl)anilineHCID 44120642—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product5-Chloro-2-methylamino-4-(3-(trifluoromethyl)piperidin-1-yl)anilineHCID 67957692—

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 4-chloro-N-methyl-2-nitro-5-(3-(trifluoromethyl)piperidin-1-yl)aniline (250 mg, 0.7 mmol), THF (6 mL), MeOH (6 mL) and Pt/C (50 mg) was stirred for 4 h at 35° C. under a hydrogen atmosphere (3.2 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-71f6b0c2434641a285de8a63bb4fc3f4
Source noteuspto-grants-2013_06