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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967484Generated: October 30, 2026

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

https://huagongshe.com/reaction/1967484

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 two 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 11 mL of concentrated hydrochloric acid (1.0 equiv.). The resulting mixture was stirred under reflux for 3.5 hours. Approximately a half amount of solvent was removed under reduced pressure. Tert-butyl methyl ether (MTBE, 900 mL) was added with vigorous stirring. The precipitate was collected by filtration and washed with a mixture of MeOH-MTBE (1:10). The product was dried in an over at 60° C. overnight under vacuum to afford a tan 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-157f4691f3a944a89a0512d9b63cad2f
Source noteuspto-grants-2013_04