Reaktion #435892

Reaktionsgleichung

acetic acid

cyclohexanone

sodium cyanoborohydride

compound

N1-(4-{[(1H-imidazol-2-ylmethyl)-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-N1-methyl-butan-1,4-diamine

→

N-cyclohexyl-N′-(4-{[(1H-imidazol-2-ylmethyl)-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-benzyl)-N′-methyl-butane-1,4-diamine

Lösungsmittel

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter the reaction
2. 2
   workup.DISTILLATIONthe solvent was distilled off
3. 3
   workup.ADDITIONSubsequently, the residue was added with a 1 mol/l sodium hydroxide aqueous solution (3.0 ml)
4. 4
   Extraktionfollowed by extraction with chloroform
5. 5
   TrocknenThe extract was dried with magnesium sulfate
6. 6
   workup.DISTILLATIONthe solvent was then distilled off
7. 7
   SonstigeThe residue was purified through silica gel column chromatography (chloroform/methanol)
8. 8
   workup.ADDITIONtreated with hydrochloric acid

Vorschrift

The compound (110.0 mg) obtained in Example 103-7 was dissolved in anhydrous methanol (4.4 ml). Then, the solution was added with cyclohexanone (0.058 ml) and sodium cyanoborohydride (52.8 mg) and adjusted to pH 5 with acetic acid, followed by stirring at room temperature for 16.5 hours. After the reaction, the solvent was distilled off. Subsequently, the residue was added with a 1 mol/l sodium hydroxide aqueous solution (3.0 ml), followed by extraction with chloroform. The extract was dried with magnesium sulfate and the solvent was then distilled off. The residue was purified through silica gel column chromatography (chloroform/methanol) and then treated with hydrochloric acid, thereby obtaining hydrochloride (96.7 mg) of the subject compound as a white solid.

Quelle