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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365473Generated: October 25, 2026

1,2-Dichloroethane → 5-chloro-1-(3-chlorobenzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid {2-[3-(4-cyanobenzyl)-3H-imidazol-4-yl]ethyl}-amide

https://huagongshe.com/reaction/365473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Chloro-1-(3-chlorobenzyl)-2-oxo-1,2-dihydro-3-pyridinecarboxylic acidHCID 3780871—
ReactantHCID 178509848HCID 178509848—
SolventDimethylformamideHCID 6228—
Product5-chloro-1-(3-chlorobenzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid {2-[3-(4-cyanobenzyl)-3H-imidazol-4-yl]ethyl}-amideHCID 54312008—

Reaction Steps

5-Chloro-1-(3-chlorobenzyl)-2-oxo-1,2-dihydro-pyridine-3-carboxylic acid (0.10 g, 0.335 mmol) was dissolved in DMF (10 mL) and treated with EDC (0.077 g, 0.402 mmol), HOBT (0.054 g, 0.402 mmol), 4-cyanobenzyl histamine (0.079 g, 0.352 mmol) and NMM (0.11 mL, 1.00 mmol) and stirred at ambient temperature for 18 hr. The reaction mixture was concentrated to remove the DMF, then partitioned between EtOAc and aq saturated NaHCO3 solution, the organic layer separated, washed with brine and dried (MgSO4). The title compound was obtained upon purification by RP HPLC on a PrepPak column eluting with an acetonitrile/H2O/TFA gradient followed by neutralization with NaHCO3 and extraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127390
Source datasetuspto-grants-2000_10
ORD IDord-edb5ca1800d34bb0b19648c103b68fd9
Source noteuspto-grants-2000_10