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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837558Generated: November 3, 2026

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

https://huagongshe.com/reaction/1837558

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 4chloro-3-nitroquinoline hydrochloride (331 g, 1.35 mmol) to provide 486 g of tert-butyl N-(4-[(3-nitroquinolin-4yl)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 numberUS06784188B2
Source datasetuspto-grants-2004_08
ORD IDord-5cc432ecc70844c58c845387eb3ba2dc
Source noteuspto-grants-2004_08