Reaktion #446899

ord-298e7860ea794e348783e4fbf310c161

Reaktionsgleichung

Sc1ccc(-c2nc3n(c2-c2ccncc2)CCC3)cc1
2-(4-mercaptophenyl)-3-(4-pyridyl)-6,7-dihydro-[5H]-pyrrolo[1,2-a]imidazole
CCN(CC)CC
triethylamine
COCBr
bromomethyl methyl ether
COCSc1ccc(-c2nc3n(c2-c2ccncc2)CCC3)cc1
desired titled compound
COCSc1ccc(-c2nc3n(c2-c2ccncc2)CCC3)cc1
2-(4-Methoxymethylthiophenyl]3-(4-pyridyl) 6,7-dihydro[5H]pyrrolo[1,2-a]imidazole

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturTo an ice bath cooled solution
  2. 2
    workup.ADDITIONcontaining

Vorschrift

To an ice bath cooled solution containing 1.0 q (3.4mmole) of 2-(4-mercaptophenyl)-3-(4-pyridyl)-6,7-dihydro-[5H]-pyrrolo[1,2-a]imidazole prepared as in Example 16 and 0.5 ml (3.6 mmole) of triethylamine in 10ml of methylene chloride is added 0.27 ml (3.5 mmole) of bromomethyl methyl ether. The reaction is allowed to warm to room temperature and stirred at room temperature for several hours. Workup and chromatography in a manner analogous to that outlined in example 18 affords the desired titled compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05002941uspto-grants-1991_03