Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47487Generated: October 26, 2026

9-Fluorenylmethyl chloroformate → 9H-9-fluorenylmethyl N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]carbamate

https://huagongshe.com/reaction/47487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
Reactant4-(4-amino-2-butyl 1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamineHCID 12992616—
Product9H-9-fluorenylmethyl N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]carbamateHCID 1201853170.8%

Reaction Steps

Using the general method of Example 55, 9-fluorenylmethyl chloroformate (0.085 g, 0.33 mmol) was reacted with 4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamine (0.105 g, 0.33 mmol) to provide 0.125 g of 9H-9-fluorenylmethyl N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]carbamate as a white powder. Analysis: Calculated for C32H34N6O2+¼H2O: %C, 71.29; %H, 6.45; %N, 15.59. Found: %C, 70.99; %H, 6.35; %N, 15.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699878B2
Source datasetuspto-grants-2004_03
ORD IDord-59a44c3dbf5342a19ced7717234b0211
Source noteuspto-grants-2004_03