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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47488Generated: October 28, 2026

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

https://huagongshe.com/reaction/47488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant4-(4-amino-2-butyl 1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamineHCID 12992616—
Productethyl N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]carbamateHCID 1298786581.3%

Reaction Steps

Using the general method of Example 55, ethyl chloroformate (46 μL, 0.48 mmol) was reacted with 4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butaneamine (0.15 g, 0.48 mmol) to provide 0.15 g of ethyl 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 C20H28N6O2: %C, 62.48; %H, 7.34; %N, 21.86. Found: %C, 61.73; %H, 7.28; %N, 21.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699878B2
Source datasetuspto-grants-2004_03
ORD IDord-e01767377a7f4e5599ce3b4c8ca4b507
Source noteuspto-grants-2004_03