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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256773생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/256773

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물1,3-Thiazole-2-carboxylic acidHCID 2762733—
반응물4-(1-(2-Fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarboxylic acidHCID 19785560—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물4-(1-(2-Fluoro-4-biphenylyl)ethyl)-2-methylamino-5-thiazolecarbohydroxamic acidHCID 1978555348.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258396
출처 데이터셋uspto-grants-1993_11
ORD IDord-bda1daba9d21467684c7ef2c7cc1ca2f
출처 메모uspto-grants-1993_11