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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1885313생성일: 2026년 10월 24일

Triethylamine → N-[4-(1-(2-Methoxyphenyl)-4-piperazinyl)-2-butynyl]-1,2-benzisothiazole-3-carboxamide dihydrochloride

https://huagongshe.com/ko/reaction/1885313

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(2-Methoxyphenyl)-4-(4-amino-2-butynyl)piperazineHCID 15329895—
반응물Benzo[d]isothiazole-3-carbonyl chlorideHCID 15639471—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-[4-(1-(2-Methoxyphenyl)-4-piperazinyl)-2-butynyl]-1,2-benzisothiazole-3-carboxamide dihydrochlorideHCID 1975229990.9%

반응 단계

A mixture of 1,2-benzisothiazole-3-carboxylic acid chloride (2.0 g) and 1-(2-methoxyphenyl)-4-(4-amino-2-butynyl)piperazine (2.63 g) in dichloromethane (100 ml), was stirred while triethylamine (2.83 ml) was added dropwise. Stirring was continued overnight. After 24 hr, the reaction mixture was diluted with water and extracted with dichloromethane. The organic phase was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica using ethyl acetate as the eluent. The appropriate fractions were collected and concentrated. The residue was taken up in ether/dichloromethane. Ethereal hydrogen chloride was added. The precipitate was recrystallized from methanol/dichloromethane/ether to provide 2.27 g (45.7%) of product, mp 162°-164° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05143923
출처 데이터셋uspto-grants-1992_09
ORD IDord-8d5d7ed35939478fa17933ed4ec4c2fd
출처 메모uspto-grants-1992_09