تفاعل #9556

ord-7c4ba5b0737a4f89b2ca5ce53f1a44b3

معادلة التفاعل

CC(C)(O)CNc1c(N)cnc2cc(Cc3ccccc3)ccc12
1-(3-amino-7-benzylquinolin-4-ylamino)-2-methylpropan-2-ol
CC(C)(O)CNc1c(N)cnc2ccc(Cc3ccccc3)cc12
1-(3-amino-6-benzylquinolin-4-ylamino)-2-methylpropan-2-ol
CCOC(OCC)OCC
triethyl orthoformate
CC(C)(O)Cn1cnc2cnc3cc(Cc4ccccc4)ccc3c21
1-(7-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol
CC(C)(O)Cn1cnc2cnc3ccc(Cc4ccccc4)cc3c21
1-(8-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction was heated
  2. 2
    درجة الحرارةat reflux for one hour
  3. 3
    أخرىA precipitate formed
  4. 4
    أخرىwhich was isolated by filtration

الإجراء التجريبي

For Examples 431 and 434, a modification of the method described in Part B of Examples 427–429 was used to treat 1-(3-amino-7-benzylquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(3-amino-6-benzylquinolin-4-ylamino)-2-methylpropan-2-ol with triethyl orthoformate, as indicated in the table below. The reaction was heated at reflux for one hour and then stirred overnight at ambient temperature. A precipitate formed, which was isolated by filtration to provide 1-(7-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol or 1-(8-benzyl-1H-imidazo[4,5-c]quinolin-1-yl)-2-methylpropan-2-ol.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091214B2uspto-grants-2006_08