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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848708Generated: October 31, 2026

4-Bromobenzylamine → N-(4-Bromobenzyl)-5-((5-methylpyridin-2-yl)methoxy)-2-nitroaniline

https://huagongshe.com/reaction/1848708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzylamineHCID 77571—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-((3-Fluoro-4-nitrophenoxy)methyl)-5-methylpyridineHCID 90411084—
SolventAcetonitrileHCID 6342—
ProductN-(4-Bromobenzyl)-5-((5-methylpyridin-2-yl)methoxy)-2-nitroanilineHCID 9041017386.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-((3-fluoro-4-nitrophenoxy)methyl)-5-methylpyridine (2.0 g, 7.6 mmol), 4-bromobenzyl amine (1.6 g, 8.4 mmol), DIPEA (2.63 mL, 15.3 mmol) and acetonitrile (25.4 mL) were sealed in a reaction vessel and heated to 60° Celsius for 24 h. The mixture was cooled to RT, transferred to a round bottomed flask and concentrated to dryness. The crude mixture was heated to 70° Celsius in a minimum amount of i-PrOH until homogeneous and cooled to RT. The resulting mixture was filtered to collect the yellow solids which were dried to afford the title compound (2.82 g, 86%). MS (ESI): mass calcd. for C20H18BrN3O3, 427.053; m/z found, 428.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952177B2
Source datasetuspto-grants-2015_02
ORD IDord-b886f18200164e86a4cf797a9c60e2e2
Source noteuspto-grants-2015_02