(3R,7S,8S,8aR)-8-ethyl-7-[(2-indolyl)ethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

Base Information

Chemical Name:(3R,7S,8S,8aR)-8-ethyl-7-[(2-indolyl)ethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine
CAS No.:1273047-59-8
Molecular Formula:C₂₅H₂₈N₂O₂
Molecular Weight:388.51
Hs Code.:

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

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

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

There total 7 articles about (3R,7S,8S,8aR)-8-ethyl-7-[(2-indolyl)ethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine 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: 54.0%

: (3R,7S,8S,8aR)-7-[2-acetyl-2-(2-indolyl)ethyl]-8-ethyl-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

: 1273047-59-8
(3R,7S,8S,8aR)-8-ethyl-7-[(2-indolyl)ethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

Guidance literature:: With hydrogen; palladium(II) hydroxide; In ethyl acetate; at 20 ℃; for 48h; under 20686.5 Torr;
DOI:10.1002/ejoc.201001020

Reference yield:

: 4264-35-1
2-acetylindole

: 1273047-59-8
(3R,7S,8S,8aR)-8-ethyl-7-[(2-indolyl)ethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium diisopropyl amide / tetrahydrofuran; cyclohexane / 1 h / -78 °C

1.2: 24 h / -78 - 20 °C

2.1: sodium tetrahydroborate / tetrahydrofuran / 4 h / 0 - 20 °C

3.1: pyridine; dmap / dichloromethane / 14 h / 20 °C

4.1: hydrogen; palladium(II) hydroxide / ethyl acetate / 48 h / 20 °C / 20686.5 Torr

With pyridine; dmap; sodium tetrahydroborate; hydrogen; palladium(II) hydroxide; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane; cyclohexane; ethyl acetate;
DOI:10.1002/ejoc.201001020

Reference yield:

: 1273048-00-2
(3R,6R,7R,8S,8aR)-6-(benzyloxycarbonyl)-8-ethyl-7-[2-(2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

: 1273047-59-8
(3R,7S,8S,8aR)-8-ethyl-7-[(2-indolyl)ethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen; palladium(II) hydroxide / ethyl acetate / 24 h / 20 °C

1.2: 16 h / Reflux

2.1: sodium tetrahydroborate / tetrahydrofuran / 4 h / 0 - 20 °C

3.1: pyridine; dmap / dichloromethane / 14 h / 20 °C

4.1: hydrogen; palladium(II) hydroxide / ethyl acetate / 48 h / 20 °C / 20686.5 Torr

With pyridine; dmap; sodium tetrahydroborate; hydrogen; palladium(II) hydroxide; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1002/ejoc.201001020