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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1097608Erstellt: 24. Oktober 2026

Acetic Acid → HCID 86626308, Verbindung

https://huagongshe.com/de/reaction/1097608

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt1-((3-Aminoquinolin-4-yl)amino)-2-methylpropan-2-olHCID 14986941—
Edukt1,3-dimethoxycarbonyl-O-methylisoureaHCID 85348789—
LösungsmittelMethanolHCID 887—
ProduktHCID 86626308HCID 86626308—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08143270B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-472c74c0e8fe4f3da8c4ec9e479e1b28
Quellennotizuspto-grants-2012_03