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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301830Generated: November 1, 2026

1,2-Dichloroethane → N1-(6-Indolylcarbonyl)-N2-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]-1,2-benzenediamine

https://huagongshe.com/reaction/2301830

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthyl AcetateHCID 8857—
ReactantN2-[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl-1,2-benzenediamineHCID 10829995—
Reactant1-Benzyloxycarbonyl-6-indolecarboxylic acidHCID 15543040—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN1-(6-Indolylcarbonyl)-N2-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]-1,2-benzenediamineHCID 155430288.4%

Reaction Steps

A solution of 1-benzyloxycarbonyl-6-indolecarboxylic acid (452 mg, 1.53 mmol), N1-[[1-(4-pyridyl)piperidin-4-yl]methoxycarbonyl]-1,2-benzenediamine (500 mg, 1.53 mmol), and EDC (294 mg, 1.53 mmol) in DMF (2.5 mL) was allowed to stir overnight (about 18 h). The mixture was poured into ethyl acetate and H2O, the aqueous layer was washed with EtOAc (3×), and the combined organic extracts were washed with 1 N NaOH (2×), H2O, brine, and dried (K2CO3). Concentration and purification of the residue by flash chromatography (SiO2) followed by recrystallization (MeOH/ether) yielded 60 mg (8%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500851B2
Source datasetuspto-grants-2002_12
ORD IDord-721df05b19434d3d8400e5eb6dda123a
Source noteuspto-grants-2002_12