Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491913Generated: October 29, 2026

3-Cyclohexyl-N-(3,3-dimethyl-butyl)-3-[(5-nitro-2-phenoxy-pyridin-4-ylmethyl)-amino]-propionamide → 3-[(5-Amino-2-phenoxy-pyridin-4-ylmethyl)-amino]-3-cyclohexyl-N-(3,3-dimethyl-butyl)-propionamide

https://huagongshe.com/reaction/491913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclohexyl-N-(3,3-dimethyl-butyl)-3-[(5-nitro-2-phenoxy-pyridin-4-ylmethyl)-amino]-propionamideHCID 67023550—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3-[(5-Amino-2-phenoxy-pyridin-4-ylmethyl)-amino]-3-cyclohexyl-N-(3,3-dimethyl-butyl)-propionamideHCID 67023617—

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a Parr bottle 10% Pd/C (0.42 g) was added and cooled to −78° C., then a solution of 3-cyclohexyl-N-(3,3-dimethyl-butyl)-3-[(5-nitro-2-phenoxy-pyridin-4-ylmethyl)-amino]-propionamide (0.42 g, 0.87 mmol) in ethyl acetate (5 mL) and ethanol (20 mL) was added. The resulting mixture was subjected to hydrogen atmosphere and shaken for 3.5 h. The hydrogen was purged with nitrogen, then the reaction mixture was filtered (glass fiber filter paper) and the solvent was evaporated under reduced pressure to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531545B2
Source datasetuspto-grants-2009_05
ORD IDord-682d19bdc14149e88f2897dd0fd55aad
Source noteuspto-grants-2009_05