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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373887Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 21075785, compound

https://huagongshe.com/reaction/1373887

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 21075783HCID 21075783—
SolventDichloromethaneHCID 6344—
ProductHCID 21075785HCID 2107578596%

Reaction Steps

A solution of N-(2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)isopropylamine (334 mg, 1.18 mmol) in 10 mL of CH2Cl2 was treated with 3-chloroperoxybenzoic acid (MCPBA) (77% max., 334 mg, 1.45 mmol). After stirring for 3 h, the reaction was quenched with saturated NaHCO3 solution and extracted into CH2Cl2. The organic portion was washed with saturated NaHCO3 solution, H2O and brine. The organic portion was dried over Na2SO4, filtered and concentrated to give N-(2-butyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)isopropylamine (338 mg) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163947B2
Source datasetuspto-grants-2007_01
ORD IDord-e18416f4c79c48e9825bc1956a50bcb1
Source noteuspto-grants-2007_01