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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130875Generated: October 25, 2026

Isoamylamine → 5-{4-[(3-Methylbutylamino)methyl]phenoxy}pyrazine-2-carboxamide

https://huagongshe.com/reaction/130875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamylamineHCID 7894—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(4-Formylphenoxy)pyrazine-2-carboxamideHCID 59730188—
SolventMethanolHCID 887—
Product5-{4-[(3-Methylbutylamino)methyl]phenoxy}pyrazine-2-carboxamideHCID 5972995131.2%

Reaction Steps

Place 5-(4-formylphenoxy)pyrazine-2-carboxamide (0.150 g, 0.617 mmol), 3-methylbutylamine (0.0537 g, 0.617 mmol) and 3 Å molecular sieves in a vial. Add methanol (3.1 mL), cap and stir overnight. Add NaBH4 (in excess over two portions) and stir until the gasses stop evolving. Load the reaction mixture directly onto a 5 g ISCO® pre-load column. Dry the column in a vacuum oven at room temperature. Purify by eluting through a 10 g ISCO® column with 2.0 M NH3 in methanol, ethyl acetate and hexanes to give the title compound (0.0606 g, 31.2%): MS ES+ 315.1 (M+H)+, base peak 228.0 (M−C5H12N)+; HPLC [YMC-Pack Pro C-18 (150×4.6 mm, S-5 microm), 0.1% TFA/acetonitrile in 0.1% TFA/water at 1.0 mL/min, 5-95% over 19 min], tR=8.5 min., 96.4% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-6e084373031c430aadbf579b3ebd9e30
Source noteuspto-grants-2008_06