ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

Base Information

Chemical Name:ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate
CAS No.:1363621-43-5
Molecular Formula:C₂₂H₁₈Cl₂N₂O₄S
Molecular Weight:477.368
Hs Code.:

Synonyms:ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

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Chemical Property of ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

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Technology Process of ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

There total 6 articles about ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate 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: 12.2%

: 1363621-23-1
ethyl 2-amino-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

: 814-68-6,25189-84-8
acryloyl chloride

: 1363621-43-5
ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

Guidance literature:: ethyl 2-amino-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate; acryloyl chloride; With dmap; In tetrahydrofuran; at 0 ℃; for 10h;

With ammonia; In tetrahydrofuran; at 20 ℃; pH=8 - 9;
DOI:10.1016/j.ejmech.2012.01.007

Reference yield:

: 1363621-21-9
ethyl 3-(4-(2,6-dichlorobenzyloxy)phenyl)-3-oxopropanoate

: 1363621-43-5
ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: bromine / dichloromethane / 1 h / 10 °C

2.1: ethanol / 20 °C / Reflux

3.1: dmap / tetrahydrofuran / 10 h / 0 °C

3.2: 20 °C / pH 8 - 9

With dmap; bromine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/j.ejmech.2012.01.007

Reference yield:

: 695157-31-4
1-(4-(2,6-dichlorobenzyloxy)phenyl)ethanone

: 1363621-43-5
ethyl 2-acrylamido-4-(4-(2,6-dichlorobenzyloxy)phenyl)thiazole-5-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 4 h / Reflux

2.1: bromine / dichloromethane / 1 h / 10 °C

3.1: ethanol / 20 °C / Reflux

4.1: dmap / tetrahydrofuran / 10 h / 0 °C

4.2: 20 °C / pH 8 - 9

With dmap; bromine; sodium hydride; In tetrahydrofuran; ethanol; dichloromethane; mineral oil;
DOI:10.1016/j.ejmech.2012.01.007