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HRID 721188作成日:2026年10月25日

2-Naphthalenemethanol → 2-Naphthylmethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamate

https://huagongshe.com/reaction/721188

反応式

関与物質

役割名称HCID仕込み量
反応物2-NaphthalenemethanolHCID 74128—
反応物TriphosgeneHCID 94429—
反応物Sodium BicarbonateHCID 516892—
反応物4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylanilineHCID 21890421—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物2-Naphthylmethyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylphenyl}carbamateHCID 21890196102.1%

反応手順

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline (100 mg) was added to toluene (10 ml) and triethylamine (1 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (140 mg) in methylene chloride was then added thereto, and the mixture was heated under reflux for 10 min. Next, 2-naphthylmethanol (87 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 (160 mg, yield 90%).

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-b4f162e89e1c439489c5c9ed3d884355
出典メモuspto-grants-2006_11