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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835096Generated: November 2, 2026

2-(2-Cyano-3-methylamino-4-nitrophenyl)-2-methyl-3-oxobutyric acid ethyl ester → 2-(4-Amino-2-cyano-3-methylamino-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester

https://huagongshe.com/reaction/1835096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Cyano-3-methylamino-4-nitrophenyl)-2-methyl-3-oxobutyric acid ethyl esterHCID 12035471—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-(4-Amino-2-cyano-3-methylamino-phenyl)-2-methyl-3-oxo-butyric acid ethyl esterHCID 1106616182.3%

Reaction Steps

A solution of the above ester (10.5 g, 32.5 mmol) in EtOAc (130 mL) was hydrogenated over 10% palladium on carbon (0.5 g) at 50 psi for 24 h. The catalyst was removed by filtration through diatomaceous earth, and the filtrate was evaporated. A mixture of EtOAc/hexane (1:1, 10 mL) was added to the residue and the resulting mixture was stirred for 0.5 h. The crystals were filtered and washed with hexane to give 2-(4-amino-2-cyano-3-methylaminophenyl)-2-methyl-3-oxobutyric acid ethyl ester (7.74 g, 81%), mp 118-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770639B2
Source datasetuspto-grants-2004_08
ORD IDord-7478c08548a54cc58812bb3cd13d1375
Source noteuspto-grants-2004_08