반응식
[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5](I)=[CH:4][C:3]=1[CH3:10].CC1(C)C(C)(C)OB([C:19]2[CH:20]=[N:21][CH:22]=[N:23][CH:24]=2)O1.C([O-])([O-])=O.[Na+].[Na+]>CN(C)C=O>[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C:19]2[CH:20]=[N:21][CH:22]=[N:23][CH:24]=2)=[CH:4][C:3]=1[CH3:10]참가 물질
반응 조건
- 온도
- 60 °C
실험 절차
In a microwave vial 2-bromo-5-iodo-1,3-dimethylbenzene (1 g) and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine (665 mg) are suspended in N,N-dimethylformamide (15 mL) and Na2CO3 (4 mL of a 2 M aqueous solution). The mixture is purged for 5 minutes with argon. [1,1′-Bis(diphenylphosphino)-ferrocene]-dichloropalladium dichloromethane complex (85 mg) is added, the vial is sealed and the mixture is stirred at 60° C. for 3 hours. After cooling to room temperature the mixture is Partitioned between water and ethyl acetate. The aqueous phase is extracted with ethyl acetate and the combined organic phases are washed with brine. Then the organic phase is dried (MgSO4) and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 80:20→50:50) to give the title compound. Yield: 446 mg; LC (method 9): tR=1.05 min; Mass spectrum (ESI+): m/z=263 [M+H]+.
후처리
- customThe mixture is purged for 5 minutes with argon
- addition[1,1′-Bis(diphenylphosphino)-ferrocene]-dichloropalladium dichloromethane complex (85 mg) is added
- customthe vial is sealed
- temperatureAfter cooling to room temperature the mixture
- customis Partitioned between water and ethyl acetate
- extractionThe aqueous phase is extracted with ethyl acetate
- washthe combined organic phases are washed with brine
- dry with materialThen the organic phase is dried (MgSO4)
- concentrationconcentrated
- customThe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 80:20→50:50)
출처 및 근거
- ORD 기록
- ord-3a2e6cd4874045e79c89d12892dede3d
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08642585B2
연결된 노트
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