Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228440Generated: October 25, 2026

2-(2-Fluorophenyl)ethylamine → 5-(2-Fluoro-4-{[2-(2-fluorophenyl)ethylamino]methyl}phenoxy)pyridine-2-carboxamide

https://huagongshe.com/reaction/228440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Fluorophenyl)ethylamineHCID 643357—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-Fluoro-4-formylphenoxy)pyridine-2-carboxamideHCID 59729937—
SolventMethanolHCID 887—
Product5-(2-Fluoro-4-{[2-(2-fluorophenyl)ethylamino]methyl}phenoxy)pyridine-2-carboxamideHCID 5973011875%

Reaction Steps

Place 5-(2-fluoro-4-formylphenoxy)pyridine-2-carboxamide (Example 403, Part B) (0.650 g, 2.50 mmol), 2-fluorophenethylamine (0.382 g, 2.75 mmol) and 3 Å molecular sieves in a vial. Add methanol (12 mL), cap and stir overnight. Add NaBH4 (slight excess) and stir until the gasses stop evolving. Load the reaction mixture directly onto a 25 g ISCO® pre-load column. Dry the column in a vacuum oven at room temperature. Purify by eluting through a 40 g ISCO® column with 0% to 10% (2.0 M NH3 in methanol) in ethyl acetate to give the title compound (0.718 g, 75%): TOF MS ES+ 384.2 (M+H)+, HRMS calcd for C21H20N3O2F2 387.2032 (M+H)+, found 387.2032, time 0.52 min; HPLC [YMC-Pro pack C-18 (150×46 mm, S-5 microm), 0.05% TFA/acetonitrile in 0.05% TFA/water at 1.0 mL/min, 10-20% over 5 min, 20-95% over 18], tR=11.4 min, 100% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-f552c9d9793f4fe58d0d29071a224a0a
Source noteuspto-grants-2009_07