(+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

Base Information

Chemical Name:(+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane
CAS No.:134037-94-8
Molecular Formula:C₂₄H₂₅NO₆
Molecular Weight:423.466
Hs Code.:

Synonyms:(+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

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Chemical Property of (+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

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Technology Process of (+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

There total 5 articles about (+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane 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: 37.0%

: 100-39-0
benzyl bromide

: (+)-(2R,5S,6R)-6-[Bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

: 134037-94-8
(+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

Guidance literature:: (+)-(2R,5S,6R)-6-[Bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 1h;

benzyl bromide; In tetrahydrofuran; at -78 ℃; for 2h; Further stages.;
DOI:10.1039/b001999m

Reference yield:

: 108-59-8
malonic acid dimethyl ester

: 134037-94-8
(+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

Guidance literature:: Multi-step reaction with 2 steps

1.1: 45 percent / NaNH₂ / tetrahydrofuran; various solvent(s) / 3 h / Heating

2.1: LDA / tetrahydrofuran / 1 h / -78 °C

2.2: 37 percent / tetrahydrofuran / 2 h / -78 °C

With sodium amide; lithium diisopropyl amide; In tetrahydrofuran; 1.1: Addition / 2.1: Metallation / 2.2: Alkylation;
DOI:10.1039/b001999m

Reference yield:

: 3-phenyl-1,7a-dihydro-pyrrolo[1,2-c]oxazol-5-one

: 134037-94-8
(+)-(2R,5S,6R,7S)-7-Benzyl-6-[bis(methoxycarbonyl)methyl]-8-oxo-2-phenyl-3-oxa-1-azabicyclo[3.3.0]octane

Guidance literature:: Multi-step reaction with 2 steps

1.1: 45 percent / NaNH₂ / tetrahydrofuran; various solvent(s) / 3 h / Heating

2.1: LDA / tetrahydrofuran / 1 h / -78 °C

2.2: 37 percent / tetrahydrofuran / 2 h / -78 °C

With sodium amide; lithium diisopropyl amide; In tetrahydrofuran; 1.1: Addition / 2.1: Metallation / 2.2: Alkylation;
DOI:10.1039/b001999m