4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

Base Information

Chemical Name:4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester
CAS No.:1454302-74-9
Molecular Formula:C₁₅H₁₈N₂O₄
Molecular Weight:290.319
Hs Code.:

Synonyms:4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

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Chemical Property of 4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

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Technology Process of 4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

There total 4 articles about 4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl 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:

: 164223-35-2
ethyl 5-{[(benzyloxy)carbonyl]amino}-3-oxopentanoate

: 1454302-74-9
4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuryl dichloride / dichloromethane / 1 h / 0 - 20 °C

2: triethylamine / acetonitrile / 72 h / 20 °C

3: trifluoroborane diethyl ether / toluene / 48 h / 150 °C

4: palladium 10% on activated carbon; hydrogen / ethanol / 7 h / 20 °C / 760.05 Torr

With sulfuryl dichloride; palladium 10% on activated carbon; hydrogen; trifluoroborane diethyl ether; triethylamine; In ethanol; dichloromethane; toluene; acetonitrile;

Reference yield:

: 1246303-67-2
[3-(2,2-dimethyl-4,6-dioxo-[1,3]dioxan-5-yl)-3-oxo-propyl]-carbamic acid benzyl ester

: 1454302-74-9
4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: ethanol / 4 h / 80 °C

2: sulfuryl dichloride / dichloromethane / 1 h / 0 - 20 °C

3: triethylamine / acetonitrile / 72 h / 20 °C

4: trifluoroborane diethyl ether / toluene / 48 h / 150 °C

5: palladium 10% on activated carbon; hydrogen / ethanol / 7 h / 20 °C / 760.05 Torr

With sulfuryl dichloride; palladium 10% on activated carbon; hydrogen; trifluoroborane diethyl ether; triethylamine; In ethanol; dichloromethane; toluene; acetonitrile;

Reference yield:

: 1454302-66-9
5-benzyloxycarbonylamino-3-oxo-2-(2-phenoxy-acetoxy)-pentanoic acid ethyl ester

: 1454302-74-9
4-(2-amino-ethyl)-2-phenoxymethyl-oxazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroborane diethyl ether / toluene / 48 h / 150 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 7 h / 20 °C / 760.05 Torr

With palladium 10% on activated carbon; hydrogen; trifluoroborane diethyl ether; In ethanol; toluene;