(-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione

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Chemical Name:(-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione
CAS No.:1228313-53-8
Molecular Formula:C₂₆H₃₁N₃O₃
Molecular Weight:433.55
Hs Code.:

Synonyms:(-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione

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Chemical Property of (-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione

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Technology Process of (-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione

There total 1 articles about (-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione 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: 88.0%

: 123-75-1
pyrrolidine

: 960599-42-2
(-)-(1R,5R)-6-benzyl-8-(4-methoxybenzyl)-6,8-diazabicyclo[3.2.2]nonane-2,7,9-trione

: 1228313-53-8
(-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione

Guidance literature:: With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; at 0 - 12 ℃; optical yield given as %de; Inert atmosphere;
DOI:10.1021/jm100182p

Reference yield: 31.0%

: 1228313-53-8
(-)-(1R,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane-7,9-dione

: 1228313-54-9
(+)-(1S,2S,5R)-6-benzyl-8-(4-methoxybenzyl)-2-(pyrrolidin-1-yl)-6,8-diazabicyclo[3.2.2]nonane

Guidance literature:: With lithium borohydride; In tetrahydrofuran; diastereoselective reaction; Inert atmosphere; Cooling with ice; Reflux;
DOI:10.1021/jm100182p