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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536108Generated: October 30, 2026

Acetic Acid → Ethyl 3-{[(4,5-dimethyl-1H-benzimidazol-2-yl)methyl]amino}-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/536108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-amino-1H-pyrrole-2-carboxylateHCID 2773439—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4,5-Dimethyl-1H-benzo[d]imidazole-2-carbaldehydeHCID 45120761—
SolventMethanolHCID 887—
ProductEthyl 3-{[(4,5-dimethyl-1H-benzimidazol-2-yl)methyl]amino}-1H-pyrrole-2-carboxylateHCID 6706849127.5%

Reaction Steps

3-Amino-1H-pyrrole-2-carboxylic acid ethyl ester (0.077 g, 0.5 mmol), 4,5-dimethyl-1H-benzimidazole-2-carbaldehyde (0.130 g, 0.75 mmol) and HOAc (0.045 g, 0.75 mmol) were stirred in methanol (4 mL) followed by addition of NaCNBH3. The resulting mixture was stirred at r.t. for 16 h. The reaction mixture was neutralized with 2M NaOH and the solvent was removed in vacuo. The residue was dissolved in ethyl acetate and extracted with water. The organic layer was dried (Na2SO4) and concentrated. The crude product was purified by flash column chromatography (heptane/ethyl acetate gradient; 0 to 100% ethyl acetate), obtaining a white solid, 0.043 g (27%) of the title compound, as a tautomeric mixture (1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859568B2
Source datasetuspto-grants-2014_10
ORD IDord-68ea19a65e0c48b19874fe27ea10611a
Source noteuspto-grants-2014_10