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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431477Generated: October 27, 2026

m-Chloroperbenzoic acid → tert-butyl 2-[2-(5-oxido-1H-imidazo[4,5-c]quinolin-1yl)ethoxy]ethylcarbamate

https://huagongshe.com/reaction/431477

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl 2-[2-(1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamateHCID 21898035—
SolventDichloromethaneHCID 6344—
Producttert-butyl 2-[2-(5-oxido-1H-imidazo[4,5-c]quinolin-1yl)ethoxy]ethylcarbamateHCID 2189803284%

Reaction Steps

A solution of tert-butyl 2-[2-(1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (5.25 g, 14.7 mmol) in 200 mL of CH2Cl2 was treated with MCPBA (77%, 3.63 g, 16.3 mmol). After stirring overnight, the reaction mixture was treated with saturated NaHCO3 solution and the layers were separated. The organic portion was washed with H2O and brine then dried over Na2SO4 and concentrated to give 4.60 g of tert-butyl 2-[2-(5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate as a light brown foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660735B2
Source datasetuspto-grants-2003_12
ORD IDord-031d8aeeeb2f4bc29f0f6e194cc84ea2
Source noteuspto-grants-2003_12