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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203586Generated: October 31, 2026

tert-butyl N-(6-iodohexyl)carbamate → tert-butyl 6-{[2-(ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-8-yl]oxy}hexylcarbamate

https://huagongshe.com/reaction/2203586

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(6-iodohexyl)carbamateHCID 10616156—
Reactant2-ethoxymethyl-1-propyl-1H-imidazo[4,5-c]quinolin-8-olHCID 67051088—
Producttert-butyl 6-{[2-(ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-8-yl]oxy}hexylcarbamateHCID 68973644—

Reaction Steps

The synthesis of 2-(ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-8-ol is described in Parts A-I of Example 2. The general method described in Part L of Example 2 was followed. 2-(Ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-8-ol (4.43 g, 15.5 mmol) was treated with tert-butyl 6-iodohexylcarbamate (prepared as described in Part F of Example 45, 6.1 g, 18.6 mmol). After the work up, the crude product was not purified to yield 9.9 g of tert-butyl 6-{[2-(ethoxymethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-8-yl]oxy}hexylcarbamate as a tan waxy solid that contained DMF and dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365567B2
Source datasetuspto-grants-2016_06
ORD IDord-9f57bcfb24f144dfbcc3dcb8836a5bfc
Source noteuspto-grants-2016_06