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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382363Generated: October 25, 2026

Sodium Hydroxide → 1-benzyl-4-amino-1H-imidazole-5-carboxamide

https://huagongshe.com/reaction/382363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Amino-1-benzyl-5-imidazole carboxamide hydrochlorideHCID 18360336—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-benzyl-4-amino-1H-imidazole-5-carboxamideHCID 1400062094.2%

Reaction Steps

9.12 g (30 mol) of 4-benzylideneamino-1-benzyl-5-imidazolecarboxamide obtained was dissolved in 135 ml of tetrahydrofuran. After the addition of 15 ml of concentrated hydrochloric acid, the mixture was stirred at room temperature for two hours. The precipitate obtained was separated by filtration and washed with tetrahydrofuran to obtain 7.26 g of 4-amino-1-benzyl-5-imidazolecarboxamide hydrochloride. 7.26 g of the 4-amino-1-benzyl-5-imidazole carboxamide hydrochloride obtained was dissolved in a mixed solvent of 100 ml of methyl alcohol and 80 ml of distilled water. After the addition of 7.5 ml of 4 N aqueous solution of sodium hydroxide, the mixture was stirred at room temperature for one hour. Methanol was evaporated and the resulting precipitate separated by filtration was washed with distilled water and ethanol to obtain 5.85 g of the title compound (yield 90%) (2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310070B1
Source datasetuspto-grants-2001_10
ORD IDord-83f0dc67c0154cc49a566396b89ae717
Source noteuspto-grants-2001_10