Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1663785생성일: 2026년 10월 23일
Hydroxybenzenesulfonic acid → N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-fluorophenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide benzenesulfonate
https://huagongshe.com/ko/reaction/1663785
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydroxybenzenesulfonic acid | HCID 15619088 | — |
| 반응물 | N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-fluorophenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide | HCID 24767979 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-fluorophenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide benzenesulfonate | HCID 86630646 | 86.3% |
반응 단계
To N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-fluorophenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide (1.00 g, 2.23 mmol) was added ethanol (50 mL), and the mixture was stirred at 80° C. for 20 min. Benzenesulfonic acid monohydrate (0.41 g, 2.33 mmol) was added to the mixture, and the mixture was further stirred for 10 min. Insoluble material was removed by filtration, and the mixture was naturally cooled to room temperature. The mixture was stood at room temperature for 16 hr, and the precipitated crystals were collected by filtration and washed with ethanol. The precipitated crystals were dried under reduced pressure at 80° C. for 6 hr to give the title compound (1.17 g, 86%) as white crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08034812B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-c081c572932847fc8af515ddb365632a |
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| 출처 메모 | uspto-grants-2011_10 |
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