反应 #89823

ord-6be7badbae1a4113b8c48da03cf5a66b

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩The reaction mixture was concentrated in vacuo
  2. 2
    其他the residue was triturated with ethyl ether
  3. 3
    其他to get a yellow solid

实验过程

To tert-butyl 5-(2-(3-(2-methoxy-2-oxoacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (18 mg, 0.033 mmol) was added a solution of 1:1 TFA:CH2Cl2 (2 mL) and stirred at RT for 2 h. The reaction mixture was concentrated in vacuo and the residue was triturated with ethyl ether to get a yellow solid to afford methyl 2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenylamino)-2-oxoacetate. (15 mg, 100%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09440961B2uspto-grants-2016_09