Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848749Generated: October 29, 2026

5-((5-Methylpyridin-2-yl)methoxy)-2-nitro-N-((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)methyl)aniline → 5-((5-methylpyridin-2-yl)methoxy)-N1-((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)methyl)benzene-1,2-diamine

https://huagongshe.com/reaction/1848749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-((5-Methylpyridin-2-yl)methoxy)-2-nitro-N-((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)methyl)anilineHCID 90410442—
CatalystPlatinumHCID 23939—
SolventTetrahydrofuranHCID 8028—
Product5-((5-methylpyridin-2-yl)methoxy)-N1-((4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)methyl)benzene-1,2-diamineHCID 9041135797.3%

Reaction Steps

To a high pressure reactor were added 5-((5-methylpyridin-2-yl)methoxy)-2-nitro-N-((4′-(trifluoromethyl)-[1,1′-biphenyl]-4-yl)methyl)aniline (147 g, 297 mmol), 5% Pt/C (23.2 g, 2.97 mmol), and THF (2.5 L). The reactor was flushed with nitrogen and then stirred under an atmosphere of H2 (135 psi) for 24 h. The mixture was then filtered through celite and the filtrate was concentrated to dryness to afford the title compound as a tan solid (134 g, 97%). MS (ESI): mass calcd. for C27H24F3N3O, 463.2; m/z found, 464.1 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 8.42-8.35 (m, 1H), 7.69 (s, 4H), 7.60-7.53 (m, 2H), 7.50-7.44 (m, 3H), 7.37 (d, J=8.0, 1H), 6.66 (d, J=8.3, 1H), 6.38 (d, J=2.7, 1H), 6.27 (dd, J=8.3, 2.7, 1H), 5.08 (s, 2H), 4.36 (s, 2H), 4.13 (bs, 1H), 3.05 (bs, 2H), 2.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952177B2
Source datasetuspto-grants-2015_02
ORD IDord-fdaff57e61af4de3877ade11c198a8b0
Source noteuspto-grants-2015_02