تفاعل #73039

ord-63b69e7bbeda44119ec322bdaa6cb786

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe crude product was triturated with hot acetonitrile
  2. 2
    أخرىto provide a tan solid
  3. 3
    أخرىWhich was recrystallized from chloroform and hexanes
  4. 4
    أخرىdried at 140° C. under vacuum
  5. 5
    أخرىto provide product as an off-white solid, mp 199-200° C

الإجراء التجريبي

1-[(4-Amino-2-propyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)methyl]cyclopropanol was prepared according to the general methods of Parts D through G of Example 84 using 1-(aminomethyl)cyclopropanol in lieu of 1-(2-aminoethyl)cyclopropanol in Part D, 4-chloro-3-nitronaphthyridine in lieu of 4-chloro-3-nitroquinoline in Part D, and trimethyl orthobutyrate in lieu of triethyl orthopropionate in Part F. The crude product was triturated with hot acetonitrile to provide a tan solid. Which was recrystallized from chloroform and hexanes and dried at 140° C. under vacuum to provide product as an off-white solid, mp 199-200° C. MS (ESI) m/z 298 (M+H)+; Anal. calcd for C16H19N5O: C, 64.63; H, 6.44; N, 23.55. Found: C, 64.32; H, 6.62; N, 23.67.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541438B2uspto-grants-2013_09