{(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

Base Information

Chemical Name:{(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester
CAS No.:1444010-83-6
Molecular Formula:C₃₀H₃₈BNO₄
Molecular Weight:487.447
Hs Code.:

Synonyms:{(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

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Chemical Property of {(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

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Technology Process of {(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

There total 7 articles about {(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester 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:

: 1444009-35-1
[(1R)-1-amino-2-(3-ethylphenyl)ethyl]boronic acid (+)-pinane-2,3-diyl diester trifluoroacetate

: 2051-95-8
succinylbenzene

: 1444010-83-6
{(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

Guidance literature:: With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at -10 ℃; for 3h;

Reference yield:

: 1444010-72-3
N-((R)-2-(3-ethylphenyl)-1-((3aS,4S,6S,7aR)-3a,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)ethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine

: 1444010-83-6
{(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 0 °C

2: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 3 h / -10 °C

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In diethyl ether; N,N-dimethyl-formamide;

Reference yield:

: 1444010-70-1
(3aS,4S,6S,7aR)-2-(3-ethylbenzyl)-3a,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborole

: 1444010-83-6
{(1R)-2-(3-ethylphenyl)-1-[(4-oxo-4-phenylbutanoyl)amino]ethyl}boronic acid (+)-pinane-2,3-diyl diester

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -100 °C

1.2: -100 - 20 °C

2.1: tetrahydrofuran / -78 - 20 °C

3.1: diethyl ether / 0 °C

4.1: N-ethyl-N,N-diisopropylamine; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 3 h / -10 °C

With n-butyllithium; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;