Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2263166생성일: 2026년 10월 25일
Water → N-imidazo[1,2-b]pyridazin-6-yl-4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide
https://huagongshe.com/reaction/2263166
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 1-(4-Phenyl-1,3-thiazol-2-yl)piperazine | HCID 712468 | — |
| 반응물 | 2,2,2-Trichloroethyl imidazo[1,2-b]pyridazin-6-ylcarbamate | HCID 68777877 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-imidazo[1,2-b]pyridazin-6-yl-4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide | HCID 68778080 | 66.5% |
반응 단계
A mixture of 2,2,2-trichloroethyl imidazo[1,2-b]pyridazin-6-ylcarbamate (198 mg, 0.408 mmol), 1-(4-phenyl-1,3-thiazol-2-yl)piperazine (200 mg, 0.815 mmol) and diisopropylethylamine (0.076 ml, 0.408 mmol) in dimethylsulfoxide (2.7 ml) was stirred at 70° C. for 15 hours. Water was poured into the reaction solution, and the mixture was exacted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 110 mg (66.5%) of the desired product as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07851473B2 |
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| 출처 데이터셋 | uspto-grants-2010_12 |
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| ORD ID | ord-18d5184949fa4b83b40c7825b7ab8da9 |
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| 출처 메모 | uspto-grants-2010_12 |
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