반응식
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]=1참가 물질
8
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
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;
후처리
- 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
출처 및 근거
- ORD 기록
- ord-f8082be76d3843d5b5ac68b5abba30ad
- 출처 데이터셋
- uspto-grants-2013_07
- 특허 번호
- US08476269B2
연결된 노트
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