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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217301Generated: November 2, 2026

Water → HCID 69321088, compound

https://huagongshe.com/reaction/2217301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Piperidinecarboxylic acid, 4-(1H-benzimidazol-2-ylamino)-, ethyl esterHCID 3018455—
ReactantHCID 14327172HCID 14327172—
SolventAcetonitrileHCID 6342—
ProductHCID 69321088HCID 6932108868.3%

Reaction Steps

A mixture of ethyl 4-(1H-benzimidazol-2-ylamino)-1-piperidine-carboxylate (0.0289 mol), 7-chloro-6,7-dihydro-5H-cyclopenta[b]pyridine (0.0289 mol) and potassium carbonate (0.0867 mol) in acetonitrile (250 ml) was stirred and refluxed for 48 hours and then brought to room temperature. The reaction was carried out again using the same quantities. The mixtures were combined, poured out into H2O and extracted with EtOAc. The organic layer was separated, washed with H2O, dried (MgSO4), filtered and the solvent was evaporated. The residue (25 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH NH4OH 97/3/0.5; 20-45 μm). Two fractions were collected and their solvents were evaporated, yielding 8 g of ethyl 4-[[1-(6,7-dihydro-5H-1-pyrindin-7-yl) 1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate (interm. 22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407969B2
Source datasetuspto-grants-2008_08
ORD IDord-0d259ff327e143a3a68d55e70155d72a
Source noteuspto-grants-2008_08