反応式
C[O:2][C:3]([C:5]1[C:10]([NH2:11])=[CH:9][C:8]([C:12]([F:15])([F:14])[F:13])=[C:7](Br)[N:6]=1)=[O:4].C(Cl)Cl.[CH3:20][N:21]1[CH:25]=[C:24](B2OC(C)(C)C(C)(C)O2)[CH:23]=[N:22]1.C([O-])([O-])=O.[Cs+].[Cs+].[OH-].[Na+]>C1COCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[NH2:11][C:10]1[C:5]([C:3]([OH:2])=[O:4])=[N:6][C:7]([C:24]2[CH:23]=[N:22][N:21]([CH3:20])[CH:25]=2)=[C:8]([C:12]([F:15])([F:14])[F:13])[CH:9]=1参加物
8
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
3-Amino-6-bromo-5-trifluoromethyl-pyridine-2-carboxylic acid methyl ester (Intermediate A4) (500 mg, 1.672 mmol), PdCl2(dppf).CH2Cl2 adduct (205 mg, 0.251 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (383 mg, 1.839 mmol) and Cs2CO3 (6.69 ml, 6.69 mmol) in THF (12 ml) under N2, was heated using microwave radiation at 150° C. for 10 minutes. 2M NaOH (5 ml) was added and the mixture was stirred at RT overnight. The mixture was filtered through Celite® (filter material) and the organic solvent was removed. The resulting aqueous layer was washed with EtOAc and acidified to pH1. The product was extracted with DCM and concentrated in vacuo to afford the title compound;
後処理
- customat 150° C.
- customfor 10 minutes
- filtrationThe mixture was filtered through Celite® (filter material)
- customthe organic solvent was removed
- washThe resulting aqueous layer was washed with EtOAc
- extractionThe product was extracted with DCM
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-f8082be76d3843d5b5ac68b5abba30ad
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08476269B2
関連ノート
読み込み中…