4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

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Chemical Name:4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one
CAS No.:1450916-01-4
Molecular Formula:C₂₁H₂₀BrN₃O₄
Molecular Weight:458.311
Hs Code.:

Synonyms:4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

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Chemical Property of 4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

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Technology Process of 4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

There total 3 articles about 4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one 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: 55.0%

: 1313613-18-1
[4-(3-oxo-morpholin-4-yl)phenyl]carbamic acid benzyl ester

: 1450915-95-3
(R)-1-chloro-3-{[(4-bromophenyl)methylene]amino}propan-2-ol

: 1450916-01-4
4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

Guidance literature:: [4-(3-oxo-morpholin-4-yl)phenyl]carbamic acid benzyl ester; With lithium tert-butoxide; In dichloromethane; at 40 ℃; for 0.166667h;

(R)-1-chloro-3-{[(4-bromophenyl)methylene]amino}propan-2-ol; In dichloromethane; at 35 - 45 ℃; for 18h;

Reference yield:

: 438056-69-0
4-(4-aminophenyl)morpholin-3-one

: 1450916-01-4
4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / tetrahydrofuran; water / 0.5 h / 0 - 50 °C

2.1: lithium tert-butoxide / dichloromethane / 0.17 h / 40 °C

2.2: 18 h / 35 - 45 °C

With triethylamine; lithium tert-butoxide; In tetrahydrofuran; dichloromethane; water;

Reference yield:

: 1122-91-4
4-bromo-benzaldehyde

: 1450916-01-4
4-{ 4-[(R)-5-[(((4-bromophenyl)methylene)amino)methyl]-2-oxo-1,3-oxazolidin-3-yl]phenyl}morpholin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: ammonia / tetrahydrofuran; water / 0.25 h

1.2: 21.5 h / 22 - 45 °C

2.1: lithium tert-butoxide / dichloromethane / 0.17 h / 40 °C

2.2: 18 h / 35 - 45 °C

With ammonia; lithium tert-butoxide; In tetrahydrofuran; dichloromethane; water;