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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636628Generated: October 29, 2026

1,1-Dimethylethyl N-{2-[(3-nitro[1,5]naphthyridin-4-yl)amino]ethyl}carbamate → tert-butyl N-{2-[(3-amino[1,5]naphthyridin-4-yl)amino]ethyl}carbamate

https://huagongshe.com/reaction/636628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Dimethylethyl N-{2-[(3-nitro[1,5]naphthyridin-4-yl)amino]ethyl}carbamateHCID 22172675—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
Producttert-butyl N-{2-[(3-amino[1,5]naphthyridin-4-yl)amino]ethyl}carbamateHCID 22172710100%

Reaction Steps

1,1-Dimethylethyl N-{2-[(3-nitro[1,5]naphthyridin-4-yl)amino]ethyl}carbamate (10 g, 0.03 mol), ethyl acetate (800 mL) and platinum on carbon catalyst were combined in a Parr bottle and then the mixture was hydrogenated overnight. The reaction mixture was filtered to remove the catalyst. The filtrate was concentrated under vacuum to provide 9.1 g of 1,1-dimethylethyl N-{2-[(3-amino[1,5]naphthyridin-4-yl)amino]ethyl}carbamate as a yellow syrup. Analysis: Calculated for C15H21N5O2+0.1 CH3CO2C2H5: % C, 59.25; % H, 7.04; % N, 22.43; Found: % C, 58.96; % H, 6.87; % N, 22.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194425B1
Source datasetuspto-grants-2001_02
ORD IDord-b5b7814ab43a435bb4ebbb97b1ac53b6
Source noteuspto-grants-2001_02