(1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

Base Information

Chemical Name:(1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline
CAS No.:160847-22-3
Molecular Formula:C₂₈H₂₆N₂O₅S
Molecular Weight:502.591
Hs Code.:

Synonyms:(1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

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Chemical Property of (1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

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Technology Process of (1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

There total 4 articles about (1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline 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: 76.0%

: 160847-21-2
(1RS)-2-benzyloxycarbonyl-1-(2-hydroxyethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

: 160847-22-3
(1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

Guidance literature:: With tetrapropylammonium perruthennate; 4 A molecular sieve; 4-methylmorpholine N-oxide; In dichloromethane; Ambient temperature;
DOI:10.1055/s-1994-25669

Reference yield:

: 142656-10-8
(1RS)-2-(benzyloxycarbonyl)-1,2,3,4-tetrahydro-1-<(methoxycarbonyl)methyl>-β-carboline

: 160847-22-3
(1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / KH / tetrahydrofuran / 12 h / Ambient temperature

2: 86 percent / LiBH₄ / 1,2-dimethoxy-ethane / 24 h / Ambient temperature

3: 76 percent / molecular sieves 4A, 4-methylmorpholine N-oxide, tetrapropylammonium perruthenate / CH₂Cl₂ / Ambient temperature

With lithium borohydride; tetrapropylammonium perruthennate; 4 A molecular sieve; potassium hydride; 4-methylmorpholine N-oxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane;
DOI:10.1055/s-1994-25669

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 160847-22-3
(1RS)-2-benzyloxycarbonyl-1-(2-oxoethyl)-N-(p-toluenesulfonyl)-1,2,3,4-tetrahydro-β-carboline

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / KH / tetrahydrofuran / 12 h / Ambient temperature

2: 86 percent / LiBH₄ / 1,2-dimethoxy-ethane / 24 h / Ambient temperature

3: 76 percent / molecular sieves 4A, 4-methylmorpholine N-oxide, tetrapropylammonium perruthenate / CH₂Cl₂ / Ambient temperature

With lithium borohydride; tetrapropylammonium perruthennate; 4 A molecular sieve; potassium hydride; 4-methylmorpholine N-oxide; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane;
DOI:10.1055/s-1994-25669