Dichloromethane → HCID 22418011, Verbindung

HRID 1720287Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1720287
ClCCl.B(Br)(Br)Br.[CH3:8][O:9][C:10]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[C:18]1[CH:23]=[CH:22][C:21]([CH2:24][N:25]2[C:29]3=[N:30][CH:31]=[CH:32][C:33]([CH3:34])=[C:28]3[N:27]=[C:26]2[CH2:35][O:36]C)=[CH:20][CH:19]=1)=[O:11]>CO>[OH:36][CH2:35][C:26]1[N:25]([CH2:24][C:21]2[CH:22]=[CH:23][C:18]([C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[C:10]([O:9][CH3:8])=[O:11])=[CH:19][CH:20]=2)[C:29]2=[N:30][CH:31]=[CH:32][C:33]([CH3:34])=[C:28]2[N:27]=1

Komponenten

5

Versuchsvorschrift

50 ml (50 mmol) of a dichloromethane solution of 1M boron tribromide was added little by little dropwise to 100 ml of a dichloromethane solution of 3.3 g (8.2 mmol) of 3-[(2'-methoxycarbonyl-biphenyl-4-yl) methyl]-2-methoxymethyl-7-methyl-3H-imidazo[4,5-b]pyridine, while stirred and cooled with ice. The mixture was further stirred at a room temperature for 12 hours. Methanol was added dropwise to the product mixture, while stirred and cooled with ice, and the solvent was distilled out at a reduced pressure. The residue was mixed with water and neutralized with sodium bicarbonate. It was weakly acidified with acetic acid and decanted to remove the water. Methanol was added to the residue and distilled out at a reduced pressure. It was re-crystallized from ethanol-isopropylether to obtain 2.4 g of the intended compound.

Aufarbeitung

  1. temperaturecooled with ice
  2. stirringThe mixture was further stirred at a room temperature for 12 hours
  3. stirringwhile stirred
  4. temperaturecooled with ice
  5. distillationthe solvent was distilled out at a reduced pressure
  6. additionThe residue was mixed with water and neutralized with sodium bicarbonate
  7. customdecanted
  8. customto remove the water
  9. additionMethanol was added to the residue
  10. distillationdistilled out at a reduced pressure
  11. customIt was re-crystallized from ethanol-isopropylether

Quellen und Nachweise

ORD-Eintrag
ord-a66d5ae5895b48429a23089bc8be30ea
Quelldatensatz
uspto-grants-1996_04
Patentnummer
US05506238

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