Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583112생성일: 2026년 10월 26일
1-Propanol → 4-Chloro-5-[3-{3-(4-formylpiperazin-1-yl)-propoxy}-4-methoxybenzylamino]-3(2H)-pyridazinone
https://huagongshe.com/reaction/583112
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Propanol | HCID 1031 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4,5-Dichloro-3-hydroxypyridazine | HCID 73247 | — |
| 반응물 | 3-(3-(4-Formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamine | HCID 19689424 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-Chloro-5-[3-{3-(4-formylpiperazin-1-yl)-propoxy}-4-methoxybenzylamino]-3(2H)-pyridazinone | HCID 15859188 | 47% |
반응 단계
A mixture comprising 11.58 g of 3-[3-(4-formylpiperazin-1-yl)-propoxy]-4-methoxybenzylamine, 5.0 g of 4,5-dichloro-3(2H)-pyridazinone, 4.6 g of triethylamine, 50 ml of n-propanol and 50 ml of water, was refluxed under heating with stirring for 14 hours. The solvent was distilled off under reduced pressure, and an aqueous potassium carbonate solution was added to the obtained residue, and the mixture was extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. Then, the solvent was distilled off, and the residue was purified by silica gel column chromatography to obtain 6.21 g of the above-identified compound as slightly yellow white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05929074 |
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| 출처 데이터셋 | uspto-grants-1999_07 |
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| ORD ID | ord-8659d09b1e8e48e6a06d73e5bce93b23 |
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| 출처 메모 | uspto-grants-1999_07 |
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