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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1-(2-Methoxyphenyl)-4-(4-amino-2-butynyl)piperazine | HCID 15329895 | — |
| 반응물 | Benzo[d]isothiazole-3-carbonyl chloride | HCID 15639471 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[4-(1-(2-Methoxyphenyl)-4-piperazinyl)-2-butynyl]-1,2-benzisothiazole-3-carboxamide dihydrochloride | HCID 19752299 | 90.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05143923 |
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| 출처 데이터셋 | uspto-grants-1992_09 |
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| ORD ID | ord-8d5d7ed35939478fa17933ed4ec4c2fd |
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| 출처 메모 | uspto-grants-1992_09 |
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