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HRID 721352作成日:2026年10月26日

2-Heptanol → 1-Methylhexyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}carbamate

https://huagongshe.com/reaction/721352

反応式

関与物質

役割名称HCID仕込み量
反応物2-HeptanolHCID 10976—
反応物TriphosgeneHCID 94429—
反応物Sodium BicarbonateHCID 516892—
反応物4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物1-Methylhexyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}carbamateHCID 2189061933.8%

反応手順

4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 mg) was added to toluene (5 ml), and triethylamine (0.5 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (77 mg) in methylene chloride was then added thereto, and the mixture was heated under reflux for 10 min. Next, 2-heptanol (30 mg) was added thereto, and the mixture was further stirred with heating under reflux for 3 hr. A saturated aqueous sodium bicarbonate solution was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution, water, and saturated brine in that order. The extract was dried over sodium sulfate and was, then concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (25 mg, yield 31%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135466B2
出典データセットuspto-grants-2006_11
ORD IDord-6009c0088e894bcda9f4d2ca42e20c3b
出典メモuspto-grants-2006_11