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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967485Generated: October 31, 2026

Hydrochloric Acid → 4-(5-Amino-1-methyl-1H-benzoimidazol-2-yl)-butyric acid methyl ester hydrochloride

https://huagongshe.com/reaction/1967485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-[(2,4-Dinitro-phenyl)-methyl-carbamoyl]-butyric acid methyl esterHCID 58382807—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(5-Amino-1-methyl-1H-benzoimidazol-2-yl)-butyric acid methyl ester hydrochlorideHCID 4689938999%

Reaction Steps

A one liter Buchi reactor was charged with 42.7 g (131.4 mmol, 1.0 equiv.) of 4-[(2,4-dinitro-phenyl)-methyl-carbamoyl]-butyric acid methyl ester, 20 g of 10% palladium on carbon (4.7% weight ratio palladium vs. starting material), and 650 mL of methanol at ambient temperature. The resulting mixture was subjected to hydrogenation at 40 psi overnight, about 18 hours. HPLC indicated that the reaction was complete in about 6-7 hours (HPLC Method B). The reaction mixture was filtered through a thin layer of Celite® 540. To the filtrate was added 12 mL of concentrated hydrochloric acid (1.1 equiv.). The resulting mixture was stirred under reflux for 3.5 hours. Solvent was removed under reduced pressure, and the solids were slurried in 1800 mL of 2 vol % of Methanol/Tert-butyl methyl ether at room temperature overnight. The solids were collected by filtration. The product was dried at 45-50° C. overnight under vacuum to afford a coffee-colored solid (36.8 g, 99% yield) with a purity of 99 Area % by HPLC analysis (HPLC Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420829B2
Source datasetuspto-grants-2013_04
ORD IDord-4ccf48678d3c4ae3abf15179061c443d
Source noteuspto-grants-2013_04