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Cesium carbonate → HCID 86690474, 화합물

HRID 1026749
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HRID 1026749 반응식
Br[C:2]1[CH:7]=[C:6]([CH2:8][NH:9][CH:10]([CH3:12])[CH3:11])[CH:5]=[CH:4][N:3]=1.[F:13][C:14]1[CH:19]=[CH:18][C:17](B(O)O)=[CH:16][CH:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C(=O)([O-])O.[Na+]>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(OCC)(=O)C.O.C(O)C.C1(C)C=CC=CC=1>[F:13][C:14]1[CH:19]=[CH:18][C:17]([C:2]2[CH:7]=[C:6]([CH2:8][NH:9][CH:10]([CH3:12])[CH3:11])[CH:5]=[CH:4][N:3]=2)=[CH:16][CH:15]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 4

HCID 10796Cesium carbonateHCID 2856454-Fluorophenylboronic acidHCID 516892Sodium BicarbonateHCID 53385538N-[(2-Bromopyridin-4-yl)methyl]propan-2-amine

생성물 1

HCID 86690474HCID 86690474, 화합물수율 53%

시약·촉매·용매 5

HCID 178418397
HCID 178418397, 화합물
촉매
HCID 702Ethanol용매
HCID 962Water용매
HCID 1140Toluene용매
HCID 8857Ethyl Acetate용매

반응 조건

온도
150 °C

실험 절차

A mixture of N-[(2-bromopyridin-4-yl)methyl]propan-2-amine (2.00 g), 4-fluorophenylboronic acid (1.34 g), cesium carbonate (4.26 g), tetrakis(triphenylphosphine)palladium (1.01 g), toluene (4.5 mL), ethanol (4.5 mL) and water (3.0 mL) was stirred under irradiation with microwave while heating at 150° C. for 30 min. Saturated aqueous sodium hydrogen carbonate solution and ethyl acetate were added to the reaction mixture, and the resulting mixture was then filtered through Celite and extracted with ethyl acetate. The whole organic phase was collected and dried over magnesium sulfate. After the desiccant was filtered off, the solution was concentrated under reduced pressure. The resulting residue was purified by column chromatography (silica gel cartridge, chloroform:methanol=96:4-92:8) and (NH silica gel cartridge, hexane:ethyl acetate=90:10-60:40) to afford the title compound (1.13 g).

후처리

  1. filtrationthe resulting mixture was then filtered through Celite
  2. extractionextracted with ethyl acetate
  3. customThe whole organic phase was collected
  4. dry with materialdried over magnesium sulfate
  5. filtrationAfter the desiccant was filtered off
  6. concentrationthe solution was concentrated under reduced pressure
  7. customThe resulting residue was purified by column chromatography (silica gel cartridge, chloroform:methanol=96:4-92:8) and (NH silica gel cartridge, hexane:ethyl acetate=90:10-60:40)

출처 및 근거

ORD 기록
ord-e92c977e3fae4cef8c68e551f184cff5
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729271B2

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