Реакция #49288

ord-9b10dc33d0c54454ab18f041a0257c0f

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеfollowed by purification by preparative thin-layer chromatography (chloroform/acetone=12/1)

Методика

In a similar manner to Step 3 of Example 1, 4-chloro-7-(1-(tert-butoxycarbonyl)indol-2-yl)isoindolinone (39.3 mg, 0.103 mmol) was dissolved in methanol (3.9 mL), and the solution was treated with 10% hydrogen chloride-methanol solution (3.9 mL), followed by purification by preparative thin-layer chromatography (chloroform/acetone=12/1) to obtain Compound 16 (24 mg, yield 83%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745641B2uspto-grants-2010_06