(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Base Information

Chemical Name:(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane
CAS No.:124268-82-2
Molecular Formula:C₃₅H₄₇N₃O₄Si
Molecular Weight:601.861
Hs Code.:

Synonyms:(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

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Chemical Property of (-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

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Technology Process of (-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

There total 22 articles about (-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane 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: 10.0%

: 116005-53-9
(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 124268-82-2,124339-55-5
(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 124268-82-2
(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Guidance literature:: With water; lithium chloride; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 100 - 105 ℃; for 2h;

Reference yield: 10.0%

: 116005-53-9
(+)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-3-(R)(carbometoxy)-2,5-diketo-3-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 124268-82-2,124339-55-5
(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>-2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

: 124268-82-2
(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Guidance literature:: With water; lithium chloride; In N,N,N,N,N,N-hexamethylphosphoric triamide; at 100 - 105 ℃; for 2h;

Reference yield:

: 87-52-5
3-(Dimethylaminomethyl)indole

: 124268-82-2
(-)-6-(R)-<(2E)-4-<(tert-butyldimethylsilyl)oxy>3-methylbut-2-enyl>2,5-diketo-3-(R)-<(3-indolyl)methyl>-4-(4-methoxybenzyl)-1,4-diazabicyclo<4.3.0>nonane

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / tri-n-butylphosphine / acetonitrile / 7 h / Heating

2: 10 percent / lithium chloride, H₂O / hexamethylphosphoric acid triamide / 2 h / 100 - 105 °C

With tributylphosphine; water; lithium chloride; In N,N,N,N,N,N-hexamethylphosphoric triamide; acetonitrile;