돌아가기
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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-(2-aminoethyl)acetamideHCID 66082—
반응물6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinoneHCID 86600915—
용매AcetoneHCID 180—
용매ChloroformHCID 6212—
생성물N-(2-{[3-amino-6-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-5-phenyl-2-pyrazinyl]amino}ethyl)acetamideHCID 69331463—

반응 조건

온도122.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265120B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-a0c9a8dc9b8740599cd55d0e4ed6d6f9
출처 메모uspto-grants-2007_09