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HRID 1097608作成日:2026年10月24日

Acetic Acid → HCID 86626308、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物p-Toluenesulfonic acidHCID 6101—
反応物HCID 14986941HCID 14986941—
反応物1,3-dimethoxycarbonyl-O-methylisoureaHCID 85348789—
溶媒MethanolHCID 887—
生成物HCID 86626308HCID 86626308—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143270B2
出典データセットuspto-grants-2012_03
ORD IDord-472c74c0e8fe4f3da8c4ec9e479e1b28
出典メモuspto-grants-2012_03