반응식
[Cl:1][C:2]1[CH:19]=[CH:18][C:5]2[C:6]([NH:9][C:10]3[CH:15]=[CH:14][C:13]([CH2:16][CH3:17])=[CH:12][CH:11]=3)=[N:7][O:8][C:4]=2[C:3]=1[C:20](O)=[O:21].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[N:47]1[CH:52]=[C:51]([NH2:53])[CH:50]=[N:49][CH:48]=1>CN(C=O)C>[Cl:1][C:2]1[CH:19]=[CH:18][C:5]2[C:6]([NH:9][C:10]3[CH:11]=[CH:12][C:13]([CH2:16][CH3:17])=[CH:14][CH:15]=3)=[N:7][O:8][C:4]=2[C:3]=1[C:20]([NH:53][C:51]1[CH:52]=[N:47][CH:48]=[N:49][CH:50]=1)=[O:21]참가 물질
반응 조건
- 온도
- 50 °C
실험 절차
6-Chloro-3-(4-ethylphenylamino)benzo[d]isoxazole-7-carboxylic acid (0.195 g, 0.615 mmol) was dissolved in DMF, followed by TEA (0.223 ml, 1.61 mmol) and HATU (0.285 g, 0.749 mmol). The mixture was allowed to stir for 5 min before adding pyrimidin-5-amine (0.0509 g, 0.535 mmol) and the mixture was heated to 50° C. overnight. The mixture was then cooled to RT, partitioned between EtOAc/brine, the layers were separated, and the aqueous was extracted with EtOAc (3×). The combined organics were washed with H2O and brine, filtered and concentrated. The crude material was purified by silica gel chromatography using 20:1 DCM/MeOH to give 6-Chloro-3-(4-ethylphenylamino)-N-(pyrimidin-5-yl)benzo[d]isoxazole-7-carboxamide as a light brown solid. MS calculated 393.8, found M+H+=394.1.
후처리
- temperatureThe mixture was then cooled to RT
- custompartitioned between EtOAc/brine
- customthe layers were separated
- extractionthe aqueous was extracted with EtOAc (3×)
- washThe combined organics were washed with H2O and brine
- filtrationfiltered
- concentrationconcentrated
- customThe crude material was purified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-1ce198f69a904c0eabcad9423edb3693
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07872128B2
연결된 노트
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