Carbamic acid, [[4-[[[[5-chloro-2-oxo-6-phenyl-3-[(2-phenylethyl)amino]-1(2H)-pyrazinyl] acetyl]amino]methyl]phenyl]iminomethyl]-, phenylmethyl ester

Base Information

Chemical Name:Carbamic acid, [[4-[[[[5-chloro-2-oxo-6-phenyl-3-[(2-phenylethyl)amino]-1(2H)-pyrazinyl] acetyl]amino]methyl]phenyl]iminomethyl]-, phenylmethyl ester
CAS No.:602280-51-3
Molecular Formula:C36H33ClN6O4
Molecular Weight:649.149
Hs Code.:

Carbamic acid,
[[4-[[[[5-chloro-2-oxo-6-phenyl-3-[(2-phenylethyl)amino]-1(2H)-pyrazinyl]
acetyl]amino]methyl]phenyl]iminomethyl]-, phenylmethyl ester

Synonyms:

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Chemical Property of Carbamic acid, [[4-[[[[5-chloro-2-oxo-6-phenyl-3-[(2-phenylethyl)amino]-1(2H)-pyrazinyl] acetyl]amino]methyl]phenyl]iminomethyl]-, phenylmethyl ester

Chemical Property:

Purity/Quality:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Carbamic acid, [[4-[[[[5-chloro-2-oxo-6-phenyl-3-[(2-phenylethyl)amino]-1(2H)-pyrazinyl] acetyl]amino]methyl]phenyl]iminomethyl]-, phenylmethyl ester

There total 7 articles about Carbamic acid, [[4-[[[[5-chloro-2-oxo-6-phenyl-3-[(2-phenylethyl)amino]-1(2H)-pyrazinyl] acetyl]amino]methyl]phenyl]iminomethyl]-, phenylmethyl 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:

: benzyl amino[4-(aminomethyl)phenyl]methylenecarbamate

: 308845-87-6
2-(5-chloro-2-oxo-3-(phenethylamino)-6-phenylpyrazin-1(2H)-yl)acetic acid

: 602280-51-3
[1-Amino-1-(4-{[2-(5-chloro-2-oxo-3-phenethylamino-6-phenyl-2H-pyrazin-1-yl)-acetylamino]-methyl}-phenyl)-meth-(Z)-ylidene]-carbamic acid benzyl ester

Guidance literature:: 2-(5-chloro-2-oxo-3-(phenethylamino)-6-phenylpyrazin-1(2H)-yl)acetic acid; With polymer-bound carbodiimide reagent; benzotriazol-1-ol; In dichloromethane; N,N-dimethyl-formamide;

benzyl amino[4-(aminomethyl)phenyl]methylenecarbamate; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm030131l

Reference yield:

: 100-52-7
benzaldehyde

: 602280-51-3
[1-Amino-1-(4-{[2-(5-chloro-2-oxo-3-phenethylamino-6-phenyl-2H-pyrazin-1-yl)-acetylamino]-methyl}-phenyl)-meth-(Z)-ylidene]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: CH₂Cl₂

1.2: 1,2-dichloro-benzene

2.1: acetonitrile / 70 °C

3.1: aq. KOH / 3 h / 20 °C

4.1: 1-hydroxybenzotriazole; polymer-bound carbodiimide reagent / dimethylformamide; CH₂Cl₂

4.2: dimethylformamide; CH₂Cl₂ / 20 °C

With potassium hydroxide; polymer-bound carbodiimide reagent; benzotriazol-1-ol; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm030131l

Reference yield:

: 308845-81-0
2-(3,5-dichloro-2-oxo-6-phenylpyrazin-1(2H)-yl)acetic acid benzyl ester

: 602280-51-3
[1-Amino-1-(4-{[2-(5-chloro-2-oxo-3-phenethylamino-6-phenyl-2H-pyrazin-1-yl)-acetylamino]-methyl}-phenyl)-meth-(Z)-ylidene]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetonitrile / 70 °C

2.1: aq. KOH / 3 h / 20 °C

3.1: 1-hydroxybenzotriazole; polymer-bound carbodiimide reagent / dimethylformamide; CH₂Cl₂

3.2: dimethylformamide; CH₂Cl₂ / 20 °C

With potassium hydroxide; polymer-bound carbodiimide reagent; benzotriazol-1-ol; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm030131l