(1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

Base Information

Chemical Name:(1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane
CAS No.:312754-74-8
Molecular Formula:C₂₀H₂₁NO₃
Molecular Weight:323.392
Hs Code.:

Synonyms:(1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

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Chemical Property of (1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

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Technology Process of (1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

There total 1 articles about (1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane 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: 57.0%

: 100-52-7
benzaldehyde

: 226991-24-8
(S)-N-methoxycarbonyl-2-benzyl-2,3-dihydropyrrole

: 312754-74-8
(1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

Guidance literature:: In acetonitrile; for 6h; Irradiation;
DOI:10.1002/1521-3765(20001016)6:20<3838::AID-CHEM3838>3.0.CO;2-1

Reference yield:

: 312754-74-8
(1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

: (2S,3S,5R)-2,5-Dibenzyl-3-hydroxy-pyrrolidine-1-carboxylic acid methyl ester

Guidance literature:: With hydrogen; palladium dihydroxide; In methanol;
DOI:10.1002/1521-3765(20001016)6:20<3838::AID-CHEM3838>3.0.CO;2-1

Reference yield:

: 312754-74-8
(1R,3R,5S,7R)-N-Methoxycarbonyl-3-benzyl-6-oxa-7-phenyl-2-azabicyclo[3.2.0]heptane

: (2S,3S,5R)-N-Methyl-2,5-dibenzyl-3-pyrrolidinol

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 20 percent Pd(OH)2/C / methanol

2: 107 mg / LAH / tetrahydrofuran / 3 h / Heating

With lithium aluminium tetrahydride; hydrogen; palladium dihydroxide; In tetrahydrofuran; methanol; 1: Hydrogenolysis / 2: Reduction;
DOI:10.1002/1521-3765(20001016)6:20<3838::AID-CHEM3838>3.0.CO;2-1