tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

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Chemical Name:tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate
CAS No.:1391630-17-3
Molecular Formula:C₃₃H₄₅N₃O₆
Molecular Weight:579.737
Hs Code.:

Synonyms:tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

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Chemical Property of tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

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Technology Process of tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

There total 5 articles about tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate 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:

: 19293-62-0
p,p'-dimethoxybenzhydrylamine

: 1391630-17-3
tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: dichloromethane / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / acetonitrile / 12 h / 20 °C

3: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -78 °C / Inert atmosphere

4: sodium tris(acetoxy)borohydride / dichloromethane / 6 h / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; sodium tris(acetoxy)borohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile; 1: |Petasis Reaction;
DOI:10.1021/jm4012643

Reference yield:

: 135884-31-0
N-boc-2-pyrroleboronic acid

: 1391630-17-3
tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: dichloromethane / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / acetonitrile / 12 h / 20 °C

3: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -78 °C / Inert atmosphere

4: sodium tris(acetoxy)borohydride / dichloromethane / 6 h / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; sodium tris(acetoxy)borohydride; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetonitrile; 1: |Petasis Reaction;
DOI:10.1021/jm4012643

Reference yield:

: 1391630-16-2
tert-butyl 2-(1-((bis(4-methoxyphenyl)methyl)amino)-2-(methoxy(methyl)amino)-2-oxo-ethyl)-1H-pyrrole-1-carboxylate

: 1391630-17-3
tert-butyl 2-(1-((Bis(4-methoxyphenyl)methyl)amino)-2-(((S)-1-methoxy-4-methyl-1-oxo-pentan-2-yl)amino)ethyl)-1H-pyrrole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / -78 °C / Inert atmosphere

2: sodium tris(acetoxy)borohydride / dichloromethane / 6 h / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; sodium tris(acetoxy)borohydride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm4012643