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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 915052생성일: 2026년 10월 24일

Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate → HCID 178456633, 화합물

https://huagongshe.com/ko/reaction/915052

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamateHCID 86600908—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
용매PyridineHCID 1049—
생성물HCID 178456633HCID 17845663329.1%

반응 조건

온도82.5 °C

반응 단계

A solution of tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate (310 mg) in 10% hydrogen chloride in MeOH (3 ml) was stirred at 20-25° C. for 18 hours and the mixture was concentrated under reduced pressure to give a residue. The residue was dissolved in pyridine (1.5 ml) and heated at 80-85° C. for 10 hours. After evaporation of pyridine, the mixture was dissolved in CHCl3, washed with 1N HCl, sat. aq. NaHCO3 and brine, dried over MgSO4 and concentrated under reduced pressure to give syrup. The syrup was purified by column chromatography on silica gel eluting with a mixture of n-hexane and EtOAc (40:60 v/v) to give 6-(6-hydroxy-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone as a solid (65 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07265120B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-6dcc2126a1a142d8914a67b900e8af3f
출처 메모uspto-grants-2007_09