تفاعل #8481

ord-adab4b87712c4dafbdcd55a8abd05d2f

معادلة التفاعل

ClCC1CO1
epichlorohydrin
Cc1cccn2cc(-c3ccc(O)cc3)nc12
product
Cc1cccn2cc(-c3ccc(O)cc3)nc12
2-[4-hydroxyphenyl]-8-methylimidazo[1,2-a]pyridine
[K+].[OH-]
potassium hydroxide
Cc1cccn2cc(-c3ccc(OCC4CO4)cc3)nc12
title compound
Cc1cccn2cc(-c3ccc(OCC4CO4)cc3)nc12
2-[4-[(2,3-Epoxy)propoxy]phenyl]-8-methylimidazo[1,2-a]pyridine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحfiltered
  2. 2
    غسيلthe filtrate washed with water
  3. 3
    أخرىdried
  4. 4
    ترشيحsodium sulfate filtered
  5. 5
    أخرىevaporated

الإجراء التجريبي

The product of Step B (27 g) in methanol (500 mL) was treated with potassium hydroxide (14 g) and stirred at ambient temperature for 2 hours. To this solution was then added epichlorohydrin (9.4 mL) and the mixture stirred for an additional 48 hours. The reaction mixture was diluted with dichloromethane, filtered and the filtrate washed with water, dried, sodium sulfate filtered and evaporated to afford the title compound (18.2 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087757B2uspto-grants-2006_08