methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

Base Information

Chemical Name:methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate
CAS No.:755759-12-7
Molecular Formula:C₂₄H₂₄N₂O₄
Molecular Weight:404.466
Hs Code.:

Synonyms:methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

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Chemical Property of methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

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Technology Process of methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

There total 3 articles about methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate 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:

: 21422-40-2
methyl 1H-indole-2-acetate

: 374890-37-6
(3R,8aS)-5-oxo-3-phenyl-2,3,8,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine

: 755759-12-7
methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

: 755759-11-6
methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

Guidance literature:: methyl 1H-indole-2-acetate; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃;

(3R,8aS)-5-oxo-3-phenyl-2,3,8,8a-tetrahydro-5H-oxazolo[3,2-a]pyridine; In tetrahydrofuran; at 0 ℃;
DOI:10.1039/b400987h

Reference yield:

: 152615-80-0
(3R,8aS)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo<3,2-a>pyridine

: 755759-12-7
methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / KH / tetrahydrofuran / 1.5 h / Heating

2: 89 percent / Na₂CO₃ / toluene / 7 h / Heating

3: LDA / tetrahydrofuran; cyclohexane / 5 h / -78 °C

With potassium hydride; sodium carbonate; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; toluene;
DOI:10.1021/jo0487101

Reference yield:

: 817574-13-3
(3R,8aS)-5-oxo-3-phenyl-6-(phenylsulfinyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

: 755759-12-7
methyl (3R,7S,8aS)-α-(2-indolyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine-7-acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / Na₂CO₃ / toluene / 7 h / Heating

2: LDA / tetrahydrofuran; cyclohexane / 5 h / -78 °C

With sodium carbonate; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; toluene;
DOI:10.1021/jo0487101