(2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate

Base Information

• Chemical Name: (2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate
• CAS No.: 1133909-61-1
• Molecular Formula: C₂₃H₂₂N₂O₃
• Molecular Weight: 374.439

Synonyms:(2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate

Chemical Property of (2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate

Chemical Property:

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Technology Process of (2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate

There total 2 articles about (2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C23H24N2O4 → (2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate (1133909-61-1) + (2R,3S,12bR)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate (1133909-62-2)

Guidance literature:

With hydrogenchloride; In diethyl ether; dichloromethane; at -78 - 20 ℃; optical yield given as %de; diastereoselective reaction;

DOI:10.1002/anie.200805130

Reference yield:

C23H24N2O4 → (2R,3S,12bS)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate (1133909-61-1) + C23H22N2O3

Guidance literature:

With hydrogenchloride; In diethyl ether; dichloromethane; at -78 ℃; for 3h; optical yield given as %ee; diastereoselective reaction;

DOI:10.1002/adsc.200900686

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