تفاعل #89846

ord-5406001ed8944638a97db91749bafe2a

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe volatiles were removed in vacuo
  2. 2
    أخرىthe residue was triturated with ethyl ether
  3. 3
    أخرىThe crude product was purified
  4. 4
    أخرىprep HPLC (method 10-35_90 mins)
  5. 5
    أخرىto afford

الإجراء التجريبي

A solution of tert-butyl 5-(2-(3-(2-tert-butoxy-2-oxoethoxy)phenyl)-quinazolin-4-ylamino)-1H-indazole-1-carboxylate was stirred in CH2Cl2 (2 mL) and TFA (2 mL) for 1 h. The volatiles were removed in vacuo and the residue was triturated with ethyl ether. The crude product was purified using prep HPLC (method 10-35_90 mins) to afford to give 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)acetic acid. (0.43 mg, 0.10 mmol)

المصدر

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