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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724673Generated: October 25, 2026

Ethyl[(pyridin-3-yl)methyl]amine → 4-Chloro-3-[5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl]-N-ethyl-N-(pyridin-3-ylmethyl)benzamide

https://huagongshe.com/reaction/1724673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl[(pyridin-3-yl)methyl]amineHCID 4716480—
Reactant4-Chloro-3-[5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxoindolin-3-yl]benzoic acidHCID 18752983—
Product4-Chloro-3-[5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl]-N-ethyl-N-(pyridin-3-ylmethyl)benzamideHCID 18753004—

Reaction Steps

4-Chloro-3-[5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxoindolin-3-yl]benzoic acid, in the racemic form, is treated with N-ethyl-3-pyridylmethylamine (document WO 01/074775, example 201a) and b)). 4-Chloro-3-[5-chloro-1-(2,4-dimethoxybenzyl)-3-methyl-2-oxoindolin-3-yl]benzoic acid, in the racemic form, is described in the document WO 01/074775, in example 101. After silica chromatography, elution being carried out with a dichloromethane/methanol 90/10 mixture, the expected compound, in the racemic form, is obtained crystallized from methanol (white powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488743B2
Source datasetuspto-grants-2009_02
ORD IDord-2a8002671e604e149c2ab5f20833f384
Source noteuspto-grants-2009_02