2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

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Chemical Name:2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate
CAS No.:1446194-08-6
Molecular Formula:C₂₃H₂₅N₅O₄S
Molecular Weight:467.549
Hs Code.:

Synonyms:2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

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Chemical Property of 2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

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Technology Process of 2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

There total 3 articles about 2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate 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:

: 815574-81-3
N-ethylhydroxylamine trifluoroacetate

: 1446194-12-2
2-phenylethyl {4-[({[(Z)-cyano(phenyl)methylene]amino}oxy)methyl]-1,3-thiazol-2-yl}carbamate

: 1446194-08-6
2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

Guidance literature:: With potassium carbonate; In water; isopropyl alcohol; at 80 ℃; for 5h;

Reference yield:

: 1427201-45-3
(2Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)acetonitrile

: 1446194-08-6
2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / dichloromethane / 0.25 h / 20 °C

1.2: 5 h

2.1: potassium carbonate / isopropyl alcohol; water / 5 h / 80 °C

With pyridine; potassium carbonate; In dichloromethane; water; isopropyl alcohol;

Reference yield:

: 7541-02-8
(Z)-2-(hydroxyimino)-2-phenylacetonitrile

: 1446194-08-6
2-phenylethyl (4-{[({(2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium iodide; caesium carbonate / acetonitrile; N,N-dimethyl-formamide / 20 °C

2.1: pyridine / dichloromethane / 0.25 h / 20 °C

2.2: 5 h

3.1: potassium carbonate / isopropyl alcohol; water / 5 h / 80 °C

With pyridine; potassium carbonate; caesium carbonate; potassium iodide; In dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile;