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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540822Generated: October 30, 2026

tert-butyl N-(3-iodopropyl)carbamate → tert-butyl 3-{[1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}propylcarbamate

https://huagongshe.com/reaction/540822

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(3-iodopropyl)carbamateHCID 11231463—
Reactant1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-olHCID 136340536—
SolventWaterHCID 962—
Producttert-butyl 3-{[1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}propylcarbamateHCID 68969654—

Reaction Steps

A modification of the general method described in Part L of Example 2 was used to treat 1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-ol with tert-butyl 3-iodopropylcarbamate. The reaction mixture was diluted with water; a precipitate formed. The precipitate was isolated by filtration, washed with water and then with diethyl ether until the filtrate was clear, and dried overnight in a vacuum oven at 60° C. to yield tert-butyl 3-{[1-(2-methylpropyl)-2-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}propylcarbamate as a tan powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871782B2
Source datasetuspto-grants-2014_10
ORD IDord-68590609b98941a5b2f3555bb00dc6f3
Source noteuspto-grants-2014_10