New learning discoveries about 221352-46-1

The synthetic route of 221352-46-1 has been constantly updated, and we look forward to future research findings.

221352-46-1, 2-(tert-Butoxycarbonyl)isoindoline-1-carboxylic acid is a indole-building-block compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

To a solution ofHATU (1.83 g, 4.82 mmol) in DMF (15 mL) was added Hunig’s base(2.34 mL, 13.1 mmol). After stirring for 5 min, racemic 2-(tert-butoxycarbonyl)isoindoline-1-carboxylic acid 2-1 (1.15 g, 4.38 mmol) and ammonium chloride (1.41 g, 26.3 mmol) wereadded to the mixture. The reaction was stirred at room temperature for 18 h. The reaction waspartitioned between EtOAc (20 mL) and water (20 mL). The layers were separated and theaqueous layer was extracted with EtOAc (2 x 20 mL). The combined organic layer waswashed with brine, dried over MgS04, filtered and concentrated. The residue was purified by silica gel chromatography (IS CO 120 g column) eluting with a hexanes/EtOAc gradient (0 to100% EtOAc) to afford the title compound. LRMS mlz (M+H) 263.2 found, 263.1 required., 221352-46-1

The synthetic route of 221352-46-1 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; MERCK SHARP & DOHME CORP.; GRESHOCK, Thomas, J.; MULHEARN, James, J.; ROECKER, Anthony, J.; JIAN, Tianying; ZHOU, Gang; GUO, Liangqin; WON, Walter; ZHANG, Ting; ANAND, Rajan; STELMACH, John, E.; WANG, Deping; KIM, Ronald, M.; LAYTON, Mark, E.; BURGEY, Christopher, S.; NANTERMET, Philippe, G.; (129 pag.)WO2018/93694; (2018); A1;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles