反応式
Br[C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][NH:8]2)=[CH:4][CH:3]=1.[C:11]([O:15][C:16](=[O:18])[CH3:17])([CH3:14])([CH3:13])[CH3:12].[Li+].C[Si]([N-][Si](C)(C)C)(C)C.F[B-](F)(F)F.C(P(C(C)(C)C)C(C)(C)C)(C)(C)C>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd]>[NH:8]1[C:9]2[C:5](=[CH:4][CH:3]=[C:2]([CH2:17][C:16]([O:15][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:18])[CH:10]=2)[CH:6]=[N:7]1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 0 °C
実験手順
6-Bromo-1H-indazole (1.3 g, 6.6 mmol) and t-butylacetate (1.33 mL, 9.9 mmol) in toluene (20 mL) were degassed with argon for 15 mins. Then the mixture was cooled to 0° C. and LiHMDS (16.5 mL, 16.5 mmol, 1M in hexane) was added dropwise. Bis(dibenzylideneacetone)palladium (380 mg, 0.66 mmol) and tri-t-butyl phosphine tetrafluoroborate (383 mg, 1.32 mmol) were added and the mixture was stirred at 10° C. for 2 hours. The mixture was quenched with water (10 mL) then extracted with EtOAc (3×25 mL). The combined organic phases were washed with water (2×10 mL), brine (10 mL) and dried over sodium sulphate (Na2SO4). The filtrate was evaporated in vacuo and purified by column chromatography on silica gel (hexane:EtOAc 80:20) to afford the title compound as a white solid (65%, 1.00 g).
後処理
- customThe mixture was quenched with water (10 mL)
- extractionthen extracted with EtOAc (3×25 mL)
- washThe combined organic phases were washed with water (2×10 mL), brine (10 mL)
- dry with materialdried over sodium sulphate (Na2SO4)
- customThe filtrate was evaporated in vacuo
- custompurified by column chromatography on silica gel (hexane:EtOAc 80:20)
出典と根拠
- ORDレコード
- ord-59e9ef7a59344e28a81c5469a600d74b
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846698B2
関連ノート
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