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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182282Generated: October 30, 2026

tert-butyl N-(4-aminobutyl)carbamate → tert-Butyl (4-((3-nitroquinolin-4-yl)amino)butyl)carbamate

https://huagongshe.com/reaction/2182282

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
Reactant4-Chloro-3-nitroquinoline hydrochlorideHCID 22478992—
Producttert-Butyl (4-((3-nitroquinolin-4-yl)amino)butyl)carbamateHCID 2238176699,886.898%

Reaction Steps

Using the general method of Example 1 Part A, tert-butyl N-(4-aminobutyl)carbamate (254 g, 1.35 mol) was reacted with 4-chloro-3-nitroquinoline hydrochloride (331 g, 1.35 mmol) to provide 486 g of tert-butyl N-(4-[(3-nitroquinolin-4-yl)amino]butyl)carbamate as yellow solid. Analysis: Calculated for C18H24N4O4: % C, 59.99; % H, 6.71; % N, 15.55. Found: % C, 59.68; % H, 6.59; % N, 15.74.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897221B2
Source datasetuspto-grants-2005_05
ORD IDord-6c24fb43949c4291b96b366b28900319
Source noteuspto-grants-2005_05