Water → HCID 57930893、化合物
反応式
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:11]=[C:12]([O:15][CH3:16])[C:13]=1Br)[C:7]([O:9][CH3:10])=[O:8])[CH3:2].[CH3:17][N:18]1[CH:22]=[C:21](B2OC(C)(C)C(C)(C)O2)[CH:20]=[N:19]1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].O>COCCOC>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH:11]=[C:12]([O:15][CH3:16])[C:13]=1[C:21]1[CH:20]=[N:19][N:18]([CH3:17])[CH:22]=1)[C:7]([O:9][CH3:10])=[O:8])[CH3:2]参加物
反応条件
- 温度
- 90 °C
実験手順
Methyl 3-ethoxy-4-bromo-5-methoxybenzoate (300 mg) and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (324 mg) were dissolved in DME in a nitrogen atmosphere, and potassium phosphate (661 mg) and 1,1′-bis(diphenylphosphino)ferrocene palladium(II) chloride-CH2Cl2 complex (85 mg) were added to it at room temperature and degassed. The reaction liquid was stirred overnight at 90° C., then cooled to room temperature, water was added to it, and filtered through Celite. The filtrate was extracted with chloroform, washed with saturated saline water, and dried with sodium sulfate. Sodium sulfate was removed through filtration, the filtrate was concentrated under reduced pressure, and the residue was purified through silica gel column chromatography (hexane/ethyl acetate=100/0 to 40/60) to obtain the title compound as a white solid.
後処理
- additionwere added to it at room temperature
- customdegassed
- customThe reaction liquid
- temperaturecooled to room temperature
- filtrationfiltered through Celite
- extractionThe filtrate was extracted with chloroform
- washwashed with saturated saline water
- dry with materialdried with sodium sulfate
- customSodium sulfate was removed through filtration
- concentrationthe filtrate was concentrated under reduced pressure
- customthe residue was purified through silica gel column chromatography (hexane/ethyl acetate=100/0 to 40/60)
出典と根拠
- ORDレコード
- ord-915960f14e944017bedbde8b38959a69
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08138197B2
反応ノート
読み込み中…