Triethylamine → N-[4-(4H-Pyrazolo[5,1-c][1,4]benzodiazepin-5(10H)-ylcarbonyl)phenyl]-2-methylbenzamide

HRID 1420007Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1420007
[CH3:1][C:2]1[CH:19]=[CH:18][CH:17]=[CH:16][C:3]=1[C:4]([NH:6][C:7]1[CH:15]=[CH:14][C:10]([C:11](Cl)=[O:12])=[CH:9][CH:8]=1)=[O:5].C(N(CC)CC)C.[N:27]1[N:36]2[C:30]([CH2:31][NH:32][C:33]3[CH:40]=[CH:39][CH:38]=[CH:37][C:34]=3[CH2:35]2)=[CH:29][CH:28]=1>C(Cl)Cl.C(OCC)(=O)C>[N:27]1[N:36]2[C:30]([CH2:31][N:32]([C:11]([C:10]3[CH:14]=[CH:15][C:7]([NH:6][C:4](=[O:5])[C:3]4[CH:16]=[CH:17][CH:18]=[CH:19][C:2]=4[CH3:1])=[CH:8][CH:9]=3)=[O:12])[C:33]3[CH:40]=[CH:39][CH:38]=[CH:37][C:34]=3[CH2:35]2)=[CH:29][CH:28]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a mixture of 1.37 g of 4-[(2-methylbenzoyl)amino]benzoyl chloride in 15 ml of methylene chloride, cooled to 0° C. is added 1.5 ml of triethylamine. To the mixture is added 5 mmol of 5,10-dihydro-4H-pyrazolo[5,1-c][1,4]benzodiazepine. The reaction mixture is allowed to stir at room temperature for 48 hours and the volatiles are removed in vacuo to give a residue. The residue is dissolved in 100 ml of ethyl acetate and washed with water, 2N citric acid, aqueous NaHCO3 and brine. The solution is dried with Na2SO4 and the solvent removed in vacuo. The residue is purified by flash chromatography on silica gel with ethyl acetate-hexane to give the desired product, m.p. 142°-146° C.

Aufarbeitung

  1. customthe volatiles are removed in vacuo
  2. customto give a residue
  3. washwashed with water, 2N citric acid, aqueous NaHCO3 and brine
  4. dry with materialThe solution is dried with Na2SO4
  5. customthe solvent removed in vacuo
  6. customThe residue is purified by flash chromatography on silica gel with ethyl acetate-hexane

Quellen und Nachweise

ORD-Eintrag
ord-1a0ddebdadc74038afcae7ebff997bd4
Quelldatensatz
uspto-grants-1999_03
Patentnummer
US05889001

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