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HRID 256773作成日:2026年10月26日

Hydrochloric Acid → 4-(1-(2-Fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarbohydroxamic acid

https://huagongshe.com/reaction/256773

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DimethylformamideHCID 6228—
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物1,3-Thiazole-2-carboxylic acidHCID 2762733—
反応物4-(1-(2-Fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarboxylic acidHCID 19785560—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物4-(1-(2-Fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarbohydroxamic acidHCID 1978555348.1%

反応手順

To an ice-cooled and stirred solution of 4-(1-(2-fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarboxylic acid (5.00 g, 14.0 mmoles) and dimethylformamide (1.03 g, 14.1 mmoles) in methylene chloride (200 ml) was added dropwise oxalyl chloride (3.93 g, 31.0 mmoles) and the mixture was stirred for 40 minutes. On the other hand, hydroxylamine hydrochloride (3.91 g, 56.3 mmoles) in water (5 ml) and triethylamine (8.55 g, 84.5 mmoles) were dissolved in tetrahydrofuran (100 ml), and to the mixture was added dropwise the above-mentioned reacted solution of thiazolecarboxylic acid. After stirring for 30 minutes, the reaction mixture was acidified to pH 4 with 1M hydrochloric acid and extracted with methylene chloride. The organic layer was washed with water, dried and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to obtain the desired 4-(1-(2-fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarbohydroxamic acid (2.50 g, 6.73 mmoles, 48%) as a light brown amorphous product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258396
出典データセットuspto-grants-1993_11
ORD IDord-bda1daba9d21467684c7ef2c7cc1ca2f
出典メモuspto-grants-1993_11