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HRID 915052作成日:2026年10月26日

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

https://huagongshe.com/reaction/915052

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamateHCID 86600908—
溶媒Hydrochloric AcidHCID 313—
溶媒MethanolHCID 887—
溶媒PyridineHCID 1049—
生成物HCID 178456633HCID 17845663329.1%

反応条件

温度82.5 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07265120B2
出典データセットuspto-grants-2007_09
ORD IDord-6dcc2126a1a142d8914a67b900e8af3f
出典メモuspto-grants-2007_09