5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine → HCID 68690012, 화합물
반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]3[CH:15]=[C:14]([CH3:16])[N:13]=[C:12]([C:17]4[CH:22]=[CH:21][CH:20]=[C:19](Br)[CH:18]=4)[CH:11]=3)=[CH:9][C:4]=2[O:3][CH2:2]1.[NH2:24][C:25]1[CH:30]=[CH:29][C:28](B2OC(C)(C)C(C)(C)O2)=[CH:27][N:26]=1>>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]3[CH:15]=[C:14]([CH3:16])[N:13]=[C:12]([C:17]4[CH:18]=[C:19]([C:28]5[CH:29]=[CH:30][C:25]([NH2:24])=[N:26][CH:27]=5)[CH:20]=[CH:21][CH:22]=4)[CH:11]=3)=[CH:9][C:4]=2[O:3][CH2:2]1참가 물질
3
실험 절차
The title compound was prepared from 4-benzo[1,3]dioxol-5-yl-2-(3-bromo-phenyl)-6-methyl-pyridine (example E.91) (0.150 g, 0.407 mmol) and commercially available 2-amino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (0.099 g, 0.448 mmol) according to the general procedure VI. Obtained as a white solid (0.100 g, 64%). MS (ISP) 382.2 [(M+H)+]; mp 203° C.
출처 및 근거
- ORD 기록
- ord-4882f8b672564446acdf90c95152031a
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호