Potassium Phosphate, Tribasic → HCID 66953575、化合物
反応式
Br[C:2]1[C:3]([F:14])=[CH:4][N:5]=[C:6]2[C:11]=1[N:10]=[C:9]([O:12][CH3:13])[CH:8]=[CH:7]2.[O-]P([O-])([O-])=O.[K+].[K+].[K+].[CH2:23]([O:30][C:31](=[O:37])[NH:32][CH:33]1[CH2:36][NH:35][CH2:34]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1C=CC(P(C2C(OC3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=CC=3)=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:23]([O:30][C:31](=[O:37])[NH:32][CH:33]1[CH2:36][N:35]([C:2]2[C:11]3[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[N:10]=3)[N:5]=[CH:4][C:3]=2[F:14])[CH2:34]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1参加物
反応条件
- 温度
- 85 °C
実験手順
An oven-dried vial was charged with 8-bromo-7-fluoro-2-methoxy-[1,5]naphthyridine (commercial; 2.0 g, 7.78 mmol), palladium(II) acetate (70 mg, 0.31 mmol), DPEphos (335 mg, 0.62 mmol), K3PO4 (4.13 g, 19.45 mmol) and azetidin-3-yl-carbamic acid benzyl ester (1.68 g, 8.17 mmol). The resulting mixture was purged with argon for several min. Dioxane (25 mL) was then added via syringe and the resulting suspension was purged with argon for 3 min. The mixture was then heated at 85° C. overnight. The solvent was removed in vacuo and the residue was extracted with EA/water. The org. layer was washed with brine, dried over MgSO4 and concentrated. To the resulting solid TBME and a few drops of DCM and MeOH were added and the mixture was sonicated for 5 min and filtered to afford the title intermediate as a beige solid (2.53 g, 85%).
後処理
- customThe resulting mixture was purged with argon for several min
- additionDioxane (25 mL) was then added via syringe
- customthe resulting suspension was purged with argon for 3 min
- customThe solvent was removed in vacuo
- extractionthe residue was extracted with EA/water
- washlayer was washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated
- additionTo the resulting solid TBME and a few drops of DCM and MeOH were added
- customthe mixture was sonicated for 5 min
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-b88317b9b7a14fb7922fde8e412a06bd
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08217029B2
反応ノート
読み込み中…