(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

Base Information

Chemical Name:(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester
CAS No.:79820-46-5
Molecular Formula:C₂₉H₃₅BrN₂O₆
Molecular Weight:587.511
Hs Code.:

Synonyms:(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

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Chemical Property of (4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

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Technology Process of (4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

There total 3 articles about (4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester 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: 53.0%

: 64-17-5
ethanol

: 79820-42-1,79820-43-2
(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(2-oxo-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

: 79820-46-5
(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

: 79820-45-4
(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(3-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

Guidance literature:: With orthoformic acid triethyl ester; copper(ll) bromide; at 40 - 45 ℃;

Reference yield:

: 79820-36-3,79820-37-4
(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(2-methyl-[1,3]dioxolan-2-ylmethyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

: 79820-46-5
(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / p-TsOH / acetone / Ambient temperature

2: 38 percent / CuBr₂, CH(OEt)3 / 40 - 45 °C

With toluene-4-sulfonic acid; orthoformic acid triethyl ester; copper(ll) bromide; In acetone;

Reference yield:

: 75303-69-4,75303-70-7
Methyl-[(4R,5S)-5-(2-methyl-[1,3]dioxolan-2-ylmethyl)-1,3,4,5-tetrahydro-benzo[cd]indol-4-yl]-carbamic acid benzyl ester

: 79820-46-5
(4R,5S)-4-(Benzyloxycarbonyl-methyl-amino)-5-(1-bromo-2,2-diethoxy-propyl)-4,5-dihydro-3H-benzo[cd]indole-1-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / NaH / 1,2-dimethoxy-ethane; tetrahydrofuran / -40 - 0 °C

2: 100 percent / p-TsOH / acetone / Ambient temperature

3: 38 percent / CuBr₂, CH(OEt)3 / 40 - 45 °C

With sodium hydride; toluene-4-sulfonic acid; orthoformic acid triethyl ester; copper(ll) bromide; In tetrahydrofuran; 1,2-dimethoxyethane; acetone;