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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727414Generated: October 26, 2026

Methyl 4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)-3-nitrobenzoate → Methyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoate

https://huagongshe.com/reaction/1727414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)-3-nitrobenzoateHCID 69028187—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
ProductMethyl 3-amino-4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)benzoateHCID 69027376—

Reaction Steps

Methyl 4-({3-[methyl(2-pyridin-2-ylethyl)amino]propyl}amino)-3-nitrobenzoate (9.1 g) in solution in an ethyl acetate/methanol mixture and 10% palladium on carbon (910 mg) are added together in an autoclave. After stirring for 4 hours under a hydrogen atmosphere (3 bars), the catalyst is eliminated by filtration on Celite and the filtrate is concentrated under reduced pressure at 40° C. in order to produce the expected compound in the form of an oil (8.2 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495110B2
Source datasetuspto-grants-2009_02
ORD IDord-4bdca2e5a52745f9aabf8b131c46a284
Source noteuspto-grants-2009_02