反応式
[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]1[CH:11]=[N:12][C:13](Cl)=[CH:14][CH:15]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH:17]1([CH:23]=[CH:24]B(O)O)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1.C(Cl)Cl.C([O-])([O-])=O.[Na+].[Na+]>O1CCOCC1>[C:1]([O:5][C:6]([NH:8][CH2:9][C:10]1[CH:11]=[N:12][C:13](/[CH:24]=[CH:23]/[CH:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[CH:14][CH:15]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]参加物
反応条件
- 温度
- 90 °C
実験手順
Combine 3-(tert-butoxycarbonylamino-methyl)-6-chloropyridine (1.42 g, 5.85 mmol), 2-cyclohexylvinyl boronic acid (1.35 g, 8.78 mmol), [1,1′-bis(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with DCM (239 mg, 0.293 mmol), and 2M aqueous Na2CO3 (9.65 mL, 19.2 mmol) in 1,4-dioxane (60 mL). Purge the resulting solution with nitrogen for 5 min and heat at 90° C. overnight. Cool the reaction mixture to room temperature and partition the mixture between EtOAc and water. Separate the aqueous phase and extract twice with EtOAc. Dry the combined organic extracts over MgSO4, filter and concentrate in vacuo. Purify by chromatography on silica gel (120 g, pre-packed cartridge) eluting stepwise with hexane/EtOAc (1:0 over 5 min, 49:1 over 5 min, 19:1 over 5 min, 9:1 over 5 min and 85:15 over 5 min; 50 mL/min) to obtain the desired intermediate (1.3 g, 70%). MS (APCI+) m/z: 317 (M+H)+.
後処理
- customPurge the resulting solution with nitrogen for 5 min
- temperatureCool the reaction mixture to room temperature
- custompartition the mixture between EtOAc and water
- customSeparate the aqueous phase
- extractionextract twice with EtOAc
- dry with materialDry the combined organic extracts over MgSO4
- filtrationfilter
- concentrationconcentrate in vacuo
- customPurify by chromatography on silica gel (120 g, pre-packed cartridge)
- washeluting stepwise with hexane/EtOAc (1:0 over 5 min, 49:1 over 5 min, 19:1 over 5 min, 9:1 over 5 min and 85:15 over 5 min; 50 mL/min)
出典と根拠
- ORDレコード
- ord-9424f586a7394a96a3c87a41a5d7c978
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08680091B2
関連ノート
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