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HRID 1277807作成日:2026年10月25日

Chlorotrimethylsilane → 2-Hydroxynicotinic acid

https://huagongshe.com/reaction/1277807

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Thionyl ChlorideHCID 24386—
反応物2-(2-Oxopyrrolidin-1-yl)acetic acidHCID 3146687—
反応物6-(4-Aminophenyl)-1,2-dihydro-2-oxonicotinic acidHCID 12918956—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物2-Hydroxynicotinic acidHCID 69114—

反応手順

A suspension of 4.29 g (30 mM) of 2-oxo-1-pyrrolidineacetic acid, 2.20 ml (30 mM) of thionyl chloride, 2.32 ml (30 mM) of dimethylformamide, and 75 ml of dichloromethane was stirred with ice bath cooling for 11/4 hrs. A mixture of 4.60 g (20 mM) of 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid, 140 ml of dichloromethane, 8.4 ml (60 mM) of triethylamine, and 7.6 ml (60 mM) of chlorotrimethylsilane was stirred at room temperature for 1 hr. The silylated pyridone solution was cooled with an ice bath and the cold solution of the acid chloride was added. The reaction mixture was stirred for 4 hrs with cooling and at room temperature for 18 hrs. The reaction mixture was evaporated to a wet solid. Ethanol was added, and the mixture was evaporated. The residue was treated with water and the solid filtered. The solid was washed with water, ethanol, and ether and dried to give 6.49 g of 6-[4-[2-oxo-1-pyrrolidinyl)acetylamino]-phenyl]-1,2-dihydro-2-oxonicotinic acid; mp <320°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04278681
出典データセットuspto-grants-1981_07
ORD IDord-a3e1f707219c4227af91fbb2c5473e39
出典メモuspto-grants-1981_07