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Cesium carbonate → Tert-butyl 2-[(4-{[4-(dimethylamino)phenyl]ethynyl}phenyl)acetyl]hydrazinecarboxylate

HRID 1465440
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HRID 1465440 반응식
Br[C:2]1[CH:10]=[CH:9][C:5]([N:6]([CH3:8])[CH3:7])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C1(P(C2C=CC=CC=2)C2C3OC4C(=CC=CC=4P(C4C=CC=CC=4)C4C=CC=CC=4)C(C)(C)C=3C=CC=2)C=CC=CC=1.[C:59]([C:61]1[CH:66]=[CH:65][C:64]([CH2:67][C:68]([NH:70][NH:71][C:72]([O:74][C:75]([CH3:78])([CH3:77])[CH3:76])=[O:73])=[O:69])=[CH:63][CH:62]=1)#[CH:60]>C(#N)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:7][N:6]([CH3:8])[C:5]1[CH:9]=[CH:10][C:2]([C:60]#[C:59][C:61]2[CH:62]=[CH:63][C:64]([CH2:67][C:68]([NH:70][NH:71][C:72]([O:74][C:75]([CH3:78])([CH3:77])[CH3:76])=[O:73])=[O:69])=[CH:65][CH:66]=2)=[CH:3][CH:4]=1
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참가 물질

7

반응물 4

HCID 10796Cesium carbonateHCID 114654-bromo-N,N-dimethylanilineHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 86651837Tert-butyl 2-[(4-ethynylphenyl)acetyl]hydrazinecarboxylate

생성물 1

HCID 58181354Tert-butyl 2-[(4-{[4-(dimethylamino)phenyl]ethynyl}phenyl)acetyl]hydrazinecarboxylate수율 38.3%

시약·촉매·용매 2

HCID 178418476HCID 178418476, 화합물촉매HCID 6342Acetonitrile용매2회

실험 절차

To a mixture of 4-bromo-N,N-dimethylaniline (175 mg, 0.88 mmol), cesium carbonate (476 mg, 1.46 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (22 mg, 0.04 mmol) and bis(acetonitrile)dichloropalladium (II) (10 mg, 0.04 mmol) was added anhydrous acetonitrile (2 ml), and the mixture was stirred at room temperature for 15 mins. A solution of tert-butyl 2-[(4-ethynylphenyl)acetyl]hydrazinecarboxylate (200 mg, 0.73 mmol) in anhydrous acetonitrile (4 ml) was added, and the mixture was stirred at 80° C. for 5 hrs. After cooling, the reaction mixture was filtered, and the insoluble material was washed with ethyl acetate. The filtrate and washing solution were combined and concentrated under reduced pressure. The concentrated residue was purified by silica gel column chromatography (chloroform:methanol=97:3) to give tert-butyl 2-[(4-{[4-(dimethylamino)phenyl]ethynyl}phenyl)acetyl]hydrazinecarboxylate (110 mg, yield 38%) as a yellow solid.

후처리

  1. stirringthe mixture was stirred at 80° C. for 5 hrs
  2. temperatureAfter cooling
  3. filtrationthe reaction mixture was filtered
  4. washthe insoluble material was washed with ethyl acetate
  5. washThe filtrate and washing solution
  6. concentrationconcentrated under reduced pressure
  7. customThe concentrated residue was purified by silica gel column chromatography (chloroform:methanol=97:3)

출처 및 근거

ORD 기록
ord-4f5454c0934b4e60b06dbdc03116b095
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999989B2

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