Diisopropylamine → HCID 67026987, 화합물
반응식
Br[C:2]1[CH:3]=[C:4]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH:5]=[N:6][C:7]=1Cl.[CH:16]([B-](F)(F)F)=[CH2:17].[K+].[CH:23]1C=C(S([O-])(=O)=O)C=C(P(C2C=CC=C(S([O-])(=O)=O)C=2)C2C=CC=C(S([O-])(=O)=O)C=2)[CH:24]=1.[Na+].[Na+].[Na+].C(NC(C)C)(C)C.C(=O)(O)[O-].[Na+]>C(#N)C.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH:23]([C:2]1[CH:3]=[C:4]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH:5]=[N:6][C:7]=1[CH:16]=[CH2:17])=[CH2:24]참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 75 °C
실험 절차
To a solution of tert-butyl 5-bromo-6-chloropyridine-3-carboxylate (24.0 g, 82.0 mmol) in acetonitrile (615 mL) and water (205 mL) were added potassium vinyltrifluoroborate (33.0 g, 246 mmol) and triphenylphosphine-3,3′,3″-trisulfonic acid trisodium salt (4.20 g, 7.38 mmol). Diisopropylamine (88.0 mL, 615 mmol) was added followed by palladium(II) acetate (0.553 g, 2.46 mmol). The mixture was heated to 75° C. After 16 h, the mixture was cooled to ambient temperature and saturated sodium bicarbonate was added. The mixture was washed with dichloromethane (3×) and the combined organics were washed with water, brine, and dried with magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% dichloromethane→5% methanol/dichloromethane) gave the title compound. MS: m/z=232.3 (M+1).
후처리
- temperaturethe mixture was cooled to ambient temperature
- washThe mixture was washed with dichloromethane (3×)
- washthe combined organics were washed with water, brine
- dry with materialdried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customPurification by silica gel chromatography (100% dichloromethane→5% methanol/dichloromethane)
출처 및 근거
- ORD 기록
- ord-0b8eeb6cdf6f4da281702a1e5915713e
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08754096B2
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