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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058706Generated: November 1, 2026

HCID 22172707, compound → Tert-butyl 4-[(3-amino[1,5]naphthyridin-4-yl)amino]butylcarbamate

https://huagongshe.com/reaction/1058706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22172707HCID 22172707—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-[(3-amino[1,5]naphthyridin-4-yl)amino]butylcarbamateHCID 22172729—

Reaction Steps

1,1-Dimethylethyl N-{4-[(3-nitro[1,5]naphthyridin-4-yl)amino]butyl}carbamate (42.7 g, 0.12 mole), platinum on carbon (2 g) and ethyl acetate (500 mL) were combined and then hydrogenated on a Parr apparatus at 30 psi (2.1 Kg/cm2) hydrogen pressure for 1 hour. The catalyst was removed by filtration and rinsed with ethyl acetate. The filtrate was concentrated under vacuum to provide 1,1-dimethylethyl N-{4-[(3-amino[1,5]naphthyridin-4-yl)amino]butyl}carbamate as a bright yellow-orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518280B2
Source datasetuspto-grants-2003_02
ORD IDord-6ba641944ecc43089825d8e212d00b20
Source noteuspto-grants-2003_02