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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097608Generated: October 26, 2026

Acetic Acid → HCID 86626308, compound

https://huagongshe.com/reaction/1097608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1-((3-Aminoquinolin-4-yl)amino)-2-methylpropan-2-olHCID 14986941—
Reactant1,3-dimethoxycarbonyl-O-methylisoureaHCID 85348789—
SolventMethanolHCID 887—
ProductHCID 86626308HCID 86626308—

Reaction Steps

A mixture of 1-[(3-amino-4-quinolinyl)amino]-2-methyl-2-propanol (1.0 g, 4.3 mmol), 1,3-dimethoxycarbonyl-O-methylisourea (prepared according to the general method of Viswanathan, N. Indian Patent No. 168,784, 1.64 g, 8.64 mmol), acetic acid (1.3 g, 22 mmol), and p-toluenesulfonic acid (0.82 g, 4.3 mmol) in methanol (20 mL) was heated at reflux for 16 hours. The volatiles were removed under reduced pressure, and the residue was dissolved in chloroform (100 mL). The solution was washed sequentially with water (100 mL), aqueous sodium carbonate (100 mL of 4% w/w), water (100 mL), and brine (100 mL) and then concentrated under reduced pressure. The residue was purified by automated flash chromatography (40+M silica cartridge, eluting with 0% to 25% CMA in chloroform) followed by recrystallization from acetonitrile to provide 0.64 g of methyl [1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-2-yl]carbamate as a white solid, mp 225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143270B2
Source datasetuspto-grants-2012_03
ORD IDord-472c74c0e8fe4f3da8c4ec9e479e1b28
Source noteuspto-grants-2012_03