Реакция #89846
ord-5406001ed8944638a97db91749bafe2a
Уравнение реакции
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ДругоеThe volatiles were removed in vacuo
- 2Другоеthe residue was triturated with ethyl ether
- 3ДругоеThe crude product was purified
- 4Другоеprep HPLC (method 10-35_90 mins)
- 5Другоеto afford
Методика
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)