تفاعل #89903

ord-ed1e2bdb01f440f68adfb6a9c48e0b2e

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe solution was concentrated in vacuo
  2. 2
    أخرىthe crude product was triturated with ether
  3. 3
    ترشيحfiltered
  4. 4
    أخرىdried under vacuum

الإجراء التجريبي

TFA (4 mL) was added to 5-(2-[(3-phenyl)phenyl)-7-methoxy-6-(2-(4-methylpiperazin-1-yl)ethoxy)quinazolin-4-ylamino)-1H-indazole-1-carboxylate and the reaction was stirred at RT for 1.5 h. The solution was concentrated in vacuo and the crude product was triturated with ether and filtered, dried under vacuum to give 2-[(3-phenyl)phenyl)-N-(1H-indazol-5-yl)-7-methoxy-6-(2-(4-methylpiperazin-1-yl)ethoxy)quinazolin-4-amine (0.166 g, 0.283 mmole, 64% over two steps). MS 586.4 (M+1). HPLC retention time 5.06 mins.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09440961B2uspto-grants-2016_09