Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915069생성일: 2026년 10월 25일
Water → N-(2-{[3-amino-6-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-5-phenyl-2-pyrazinyl]amino}ethyl)acetamide
https://huagongshe.com/reaction/915069
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | N-(2-aminoethyl)acetamide | HCID 66082 | — |
| 반응물 | 6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone | HCID 86600915 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-(2-{[3-amino-6-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-5-phenyl-2-pyrazinyl]amino}ethyl)acetamide | HCID 69331463 | — |
반응 단계
A mixture of 6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone (150 mg) and N-(2-aminoethyl)acetamide (0.112 ml) in 1,2-dimethyl-2-imidazolidinone (0.3 ml) was heated at 120-125° C. for 50 hours. After addition of water (3 ml), an aqueous layer was removed by decantation to give a residue. The residue was dissolved in CHCl3, dried over MgSO4, concentrated under reduced pressure and purified by column chromatography on silica gel eluting with a mixture of MeOH and EtOAc (3:97 v/v) to give a solid. The solid was suspended in acetone to give N-(2-{[3-amino-6-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-5-phenyl-2-pyrazinyl]amino}ethyl)acetamide (28 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07265120B2 |
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| 출처 데이터셋 | uspto-grants-2007_09 |
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| ORD ID | ord-a0c9a8dc9b8740599cd55d0e4ed6d6f9 |
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| 출처 메모 | uspto-grants-2007_09 |
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