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Br[C:2]1[C:9]([CH3:10])=[CH:8][C:5]([C:6]#[N:7])=[C:4]([F:11])[CH:3]=1.C([O-])([O-])=O.[K+].[K+].[C:18]([CH2:20][C:21]1[CH:22]=[C:23](B(O)O)[CH:24]=[CH:25][CH:26]=1)#[N:19]>CN(C)C=O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:18]([CH2:20][C:21]1[CH:26]=[C:25]([C:2]2[CH:3]=[C:4]([F:11])[C:5]([C:6]#[N:7])=[CH:8][C:9]=2[CH3:10])[CH:24]=[CH:23][CH:22]=1)#[N:19]참가 물질
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- 온도
- 150 °C
실험 절차
Tetrakis(triphenylphosphine)palladium (10 mg, 0.1 mmol) was added into the solution of 4-bromo-2-fluoro-5-methylbenzonitrile (110 mg, 0.5 mmol), K2CO3 70% aqueous solution (1 mL) and 3-(cyanomethyl)phenylboronic acid (96 mg, 0.6 mmol) in 10 ml N,N-dimethyl formamide, the solution was heated at 150° C. under microwave condition for 20 minutes, and the reaction mixture was partitioned with 20 mL water and 50 mL ethyl acetate, the aqueous layer was extracted with ethyl acetate (100 mL×2), and the combined organic layer was washed by saturated solution of sodium bicarbonate, sodium chloride, and dried by sodium sulfate, and concentrated by give quantitative products 3′-(cyanomethyl)-5-fluoro-2-methylbiphenyl-4-carbonitrile 3 (114 mg, 88% yield, confirmed by LCMS: 251.10) without purification for next steps.
후처리
- customthe reaction mixture was partitioned with 20 mL water and 50 mL ethyl acetate
- extractionthe aqueous layer was extracted with ethyl acetate (100 mL×2)
- washthe combined organic layer was washed by saturated solution of sodium bicarbonate, sodium chloride
- dry with materialdried by sodium sulfate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-1de5a6f96c6c4dc4916563c43b261c6e
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08835445B2
연결된 노트
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