Реакция #89818
ord-b12b1b242b094218901563dbbe65a81f
Уравнение реакции
Реактанты
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1КонцентрированиеThe reaction mixture was concentrated in vacuo
- 2Другоеthe residue was triturated with ethyl ether
- 3Другоеto get a yellow solid
- 4ДругоеProduct was purified
- 5Другоеprep HPLC (method 25-50_70 mins)
Методика
To tert-butyl 5-(2-(3-(2-methoxyacetamido)phenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (95 mg, 0.18 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. Product was purified using prep HPLC (method 25-50_70 mins) to afford 2-methoxyacetyl chloride N-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenyl)-2-methoxyacetamide. (45 mg, 59%)