1,4-Dibromobutane → HCID 22010768, Verbindung

HRID 323156Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 323156
CC1C=CC(C2C(C(N[C:17]3[CH:33]=[CH:32][CH:31]=[CH:30][C:18]=3[C:19]([N:21]([CH3:29])[C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[OH:28])=[O:20])=O)=CC=CC=2)=CC=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:41][CH2:42][CH2:43][CH2:44]Br.[CH3:46][C:47]1[CH:52]=[CH:51][C:50]([C:53]2[C:54]([C:59]([NH:61]C3C=CC=CC=3C(N(C)C3C=CC=CC=3OCCCCBr)=O)=[O:60])=[CH:55][CH:56]=[CH:57][CH:58]=2)=[CH:49][CH:48]=1.[CH3:84][N:85]1[CH2:90][CH2:89][NH:88][CH2:87][CH2:86]1>CN(C)C=O>[CH3:46][C:47]1[CH:48]=[CH:49][C:50]([C:53]2[C:54]([C:59]([NH:61][C:32]3[CH:31]=[CH:30][C:18]([C:19]([N:21]([CH3:29])[C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=4[O:28][CH2:41][CH2:42][CH2:43][CH2:44][N:88]4[CH2:89][CH2:90][N:85]([CH3:84])[CH2:86][CH2:87]4)=[O:20])=[CH:17][CH:33]=3)=[O:60])=[CH:55][CH:56]=[CH:57][CH:58]=2)=[CH:51][CH:52]=1

Komponenten

7

Edukt 5

HCID 80561,4-DibromobutaneHCID 11430Potassium CarbonateHCID 531671-MethylpiperazineHCID 22010724HCID 22010724, VerbindungHCID 22010867HCID 22010867, Verbindung

Produkt 1

HCID 22010768HCID 22010768, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of 4′-methylbiphenyl-2-carboxamido-N-methyl-N-(2-hydroxyphenyl)benzamide (750 mg) in N,N-dimethylformamide (35 ml) was added potassium carbonate (1.42 g), 1,4-dibromobutane (1.11 g). The reaction mixture was stirred at 60° C. for 3 hours and to this mixture containing 4′-methylbiphenyl-2-carboxamido-N-methyl-N-[2-(4-bromobutoxy)phenyl]benzamide was added 1-methylpiperazine (1.03 g) and stirring was continued additional 15 hours. The mixture was extracted with ethyl acetate and washed with water and brine. The organic solution was dried over sodium sulfate. The solvent was removed by evaporation and purified by silica gel column chromatography (SiO2; 35 g, 5% methanol in dichloromethane) to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-[4-(4-methylpiperazin-1-yl)butoxy]phenyl]benzamide.

Aufarbeitung

  1. stirringstirring
  2. waitwas continued additional 15 hours
  3. extractionThe mixture was extracted with ethyl acetate
  4. washwashed with water and brine
  5. dry with materialThe organic solution was dried over sodium sulfate
  6. customThe solvent was removed by evaporation
  7. custompurified by silica gel column chromatography (SiO2; 35 g, 5% methanol in dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-49623913b1914242b01f9e072e9da212
Quelldatensatz
uspto-grants-2001_04
Patentnummer
US06211242B1

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