[1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

Base Information

Chemical Name:[1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester
CAS No.:439860-51-2
Molecular Formula:C₁₇H₁₈N₂O₃
Molecular Weight:298.342
Hs Code.:

Synonyms:[1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

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Chemical Property of [1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

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Technology Process of [1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

There total 1 articles about [1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl 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: 74.0%

: 69395-13-7
4-(2-hydroxyethyl)benzonitrile

: 501-53-1,94274-21-2
benzyl chloroformate

: 439860-51-2
[1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

Guidance literature:: 4-(2-hydroxyethyl)benzonitrile; With acetyl chloride; In ethanol; at 0 - 20 ℃;

With ammonia; In methanol; at 20 ℃;

benzyl chloroformate; With potassium carbonate; In tetrahydrofuran; water; at 20 ℃;
DOI:10.1016/S0968-0896(01)00426-6

Reference yield:

: 439860-51-2
[1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

: trans-(4R,5R)-N¹-{2-(4-[amino(imino)methyl]phenyl)ethyl}-N²-benzyl-1,3-dioxolane-4,5-dicarboxamide acetate

Guidance literature:: Multi-step reaction with 8 steps

1: pyridine / 3 h / 0 °C

2: 2.32 g / NaN₃ / dimethylformamide / 48 h / 20 °C

3: 740 mg / PPh₃ / methanol / 20 °C

4: TFA / CH₂Cl₂ / 1 h / 20 °C

5: 50 percent / HOBt; Et₃N; EDC / dimethylformamide / 0 - 20 °C / pH 7 - 8

6: aq. NaOH / dioxane; H₂O / 0.33 h / 20 °C

7: HOBt; Et₃N; EDC / dimethylformamide / 20 h / 0 °C / pH 7 - 8

8: 49 mg / H₂ / 10 percent Pd/C / ethanol / 0.75 h / 20 °C / atmospheric pressure

With sodium hydroxide; sodium azide; hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; triphenylphosphine; trifluoroacetic acid; palladium on activated charcoal; In 1,4-dioxane; pyridine; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(01)00426-6

Reference yield:

: 439860-51-2
[1-Amino-1-[4-(2-hydroxy-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

: 439860-66-9
[1-Amino-1-[4-(2-azido-ethyl)-phenyl]-meth-(Z)-ylidene]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 3 h / 0 °C

2: 2.32 g / NaN₃ / dimethylformamide / 48 h / 20 °C

With sodium azide; In pyridine; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(01)00426-6