反応式
[CH2:1]([O:3]/[CH:4]=[CH:5]/B1OC(C)(C)C(C)(C)O1)[CH3:2].P([O-])([O-])([O-])=O.[K+].[K+].[K+].C1(P(C2CCCCC2)C2C=CC=CC=2C2C(OC)=CC=CC=2OC)CCCCC1.Br[C:53]1[S:57][C:56]([C:58]2[CH:59]=[N:60][N:61]([CH3:67])[C:62]=2[C:63]([O:65][CH3:66])=[O:64])=[N:55][C:54]=1[CH3:68].C(=O)([O-])O.[Na+]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C(OCC)(=O)C.C(#N)C.O>[CH2:4]([O:3]/[CH:1]=[CH:2]/[C:53]1[S:57][C:56]([C:58]2[CH:59]=[N:60][N:61]([CH3:67])[C:62]=2[C:63]([O:65][CH3:66])=[O:64])=[N:55][C:54]=1[CH3:68])[CH3:5]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- 90 °C
実験手順
(E)-2-(2-ethoxyvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (63 mg), palladium acetate (7.1 mg), tripotassium phosphate (67 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (26 mg), and water (0.35 ml) were added to an acetonitrile (4.0 ml) solution of the methyl 4-(5-bromo-4-methylthiazol-2-yl)-1-methyl-1H-pyrazole-5-carboxylate (50 mg) obtained in (Example 5.11) <Step 1>, and the obtained mixture was then stirred under heating in a nitrogen atmosphere for 2 hours at 90° C. Thereafter, ethyl acetate (50 ml) and a saturated sodium hydrogen carbonate aqueous solution (30 ml) were added to the reaction solution. After extraction of organic layers, water layers were extracted with ethyl acetate (50 ml). The organic layers were combined. The combined organic layer was washed with a saturated saline, and was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure, and the obtained residue was then purified by silica gel column chromatography (silica gel: eluent; heptane:ethyl acetate=92:8-40:60), so as to obtain the title compound (31 mg) in the form of a yellow solid.
後処理
- customobtained in (Example 5.11) <Step 1>
- extractionAfter extraction of organic layers, water layers
- extractionwere extracted with ethyl acetate (50 ml)
- washThe combined organic layer was washed with a saturated saline
- dry with materialwas then dried over anhydrous sodium sulfate
- distillationThe solvent was distilled away under reduced pressure
- customthe obtained residue was then purified by silica gel column chromatography (silica gel: eluent; heptane:ethyl acetate=92:8-40:60)
出典と根拠
- ORDレコード
- ord-8adc4bd725a3487796553da0eed739c8
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09440970B2
関連ノート
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