13-Sep-2021 News Application of 5763-44-0

The synthetic route of 5763-44-0 has been constantly updated, and we look forward to future research findings.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 5763-44-0, name is Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione, A new synthetic method of this compound is introduced below., Product Details of 5763-44-0

tert-Butyl 4-(4-chloro-2-(2-((1,3-dioxohexahydrocyclopenta[c]pyrrol-2(1H)-yl)methyl)thieno[3,2-b]pyridin-7-yl)-6-methylphenoxy)piperidine-1-carboxylate. To diisopropyl azodicarboxylate (99 mg, 0.49 mmol) and tert-butyl 4-[4-chloro-2-[2-(hydroxymethyl)thieno[3,2-b]pyridin-7-yl]-6-methyl-phenoxy]piperidine-1-carboxylate (30 mg, 0.06 mmol) in THF (5 mL) was added triphenylphosphine polymer bound (0.55 mmol) and 4,5,6,6a-tetrahydro-3aH-cyclopenta[c]pyrrole-1,3-dione (61 mg, 0.44 mmol). Stirred at 60 C. for 2 h. The mixture was filtered and the filtrate washed twice with EtOAc. Combined all organic phases and washed with water and brine. Concentrated under vacuo and purified by column chromatography with hexanes:EtOAc (70% to 100%) to give 26 mg (69%) of the title compound as a light yellow oil. [M+H] 610.0

The synthetic route of 5763-44-0 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; FLX Bio, Inc.; Biannic, Berenger; Han, Xinping; Hu, Dennis X.; Ketcham, John Michael; Leger, Paul Robert; Maung, Jack; Okano, Akinori; Schwarz, Jacob Bradley; Shibuya, Grant; Wustrow, David Juergen; Young, Kyle; US2019/142834; (2019); A1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Application of 5763-44-0

The synthetic route of 5763-44-0 has been constantly updated, and we look forward to future research findings.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 5763-44-0, name is Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione, A new synthetic method of this compound is introduced below., Formula: C7H9NO2

tert-Butyl 4-(4-chloro-2-(2-((1,3-dioxohexahydrocyclopenta[c]pyrrol-2(1H)-yl)methyl)thieno[3,2-b]pyridin-7-yl)-6-methylphenoxy)piperidine-1-carboxylate. To diisopropyl azodicarboxylate (99 mg, 0.49 mmol) and tert-butyl 4-[4-chloro-2-[2-(hydroxymethyl)thieno[3,2-b]pyridin-7-yl]-6-methyl-phenoxy]piperidine-1-carboxylate (30 mg, 0.06 mmol) in THF (5 mL) was added triphenylphosphine polymer bound (0.55 mmol) and 4,5,6,6a-tetrahydro-3aH-cyclopenta[c]pyrrole-1,3-dione (61 mg, 0.44 mmol). Stirred at 60 C. for 2 h. The mixture was filtered and the filtrate washed twice with EtOAc. Combined all organic phases and washed with water and brine. Concentrated under vacuo and purified by column chromatography with hexanes:EtOAc (70% to 100%) to give 26 mg (69%) of the title compound as a light yellow oil. [M+H] 610.0

The synthetic route of 5763-44-0 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; FLX Bio, Inc.; Biannic, Berenger; Han, Xinping; Hu, Dennis X.; Ketcham, John Michael; Leger, Paul Robert; Maung, Jack; Okano, Akinori; Schwarz, Jacob Bradley; Shibuya, Grant; Wustrow, David Juergen; Young, Kyle; US2019/142834; (2019); A1;,
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics