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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228452Generated: October 30, 2026

p-Fluorophenethylamine → HCID 59730324, compound

https://huagongshe.com/reaction/228452

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluorophenethylamineHCID 4653—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-Fluoro-4-formylphenoxy)pyrazine-2-carboxamideHCID 59730013—
SolventMethanolHCID 887—
ProductHCID 59730324HCID 5973032465.1%

Reaction Steps

Place 5-(2-fluoro-4-formylphenoxy)pyrazine-2-carboxamide (Example 737, Part E) (0.400 g, 1.53 mmol), 4-fluorophenethylamine (0.234 g, 1.68 mmol) and 3 Å molecular-sieves in a vial. Add methanol (7.7 mL), cap and stir overnight. Add NaBH4 (0.058 g, 1.53 mmol) 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 15% (2.0 M NH3 in methanol) in 80% (ethyl acetate in hexanes). Concentrate the fractions containing the product. Take the solid up in dichloromethane (100 mL) and wash with 1.0 N NaOH (2×25 mL) to give the title compound (0.383 g, 65%): TOF MS ES+ 385.1 (M+H)+, HRMS calcd for C20H19N4O2F2 385.1476 (M+H)+, found 385.1480, time 0.55 min; HPLC [YMC-Pro pack C-18 (150×4.6 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=11.1 min, 100% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-111fd79ffaaa459da8772c7849479b7d
Source noteuspto-grants-2009_07