2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

Base Information

Chemical Name:2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester
CAS No.:1232234-91-1
Molecular Formula:C₃₀H₂₆ClN₃O₃S
Molecular Weight:544.074
Hs Code.:

Synonyms:2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

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Chemical Property of 2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

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Technology Process of 2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

There total 8 articles about 2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-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:

: 1232234-47-7
4-(3-chloro-phenyl)-2-(6-formyl-benzoimidazol-1-yl)-thiazole-5-carboxylic acid ethyl ester

: 54314-85-1
(3-benzyloxypropyl)triphenylphosphonium bromide

: 1232234-91-1
2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

Guidance literature:: (3-benzyloxypropyl)triphenylphosphonium bromide; With phenyllithium; In tetrahydrofuran; at -78 ℃;

4-(3-chloro-phenyl)-2-(6-formyl-benzoimidazol-1-yl)-thiazole-5-carboxylic acid ethyl ester; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 160538-51-2
3-fluoro-4-nitro-benzaldehyde

: 1232234-91-1
2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: toluene-4-sulfonic acid / methanol / 1 h / Reflux

2.1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 80 °C

3.1: hydrogenchloride; water / acetonitrile / 0.5 h / 60 °C

4.1: ammonium chloride; zinc / tetrahydrofuran / 1 h

5.1: acetic acid / 1 h

5.2: pH 9

6.1: phenyllithium / tetrahydrofuran / -78 °C

6.2: 20 °C

With hydrogenchloride; water; ammonium chloride; caesium carbonate; acetic acid; phenyllithium; zinc; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1H-1,3-benzodiazole-6-carbaldehyde

: 1232234-91-1
2-[6-(4-benzyloxy-but-1-enyl)-benzoimidazol-1-yl]-4-(3-chloro-phenyl)-thiazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0 °C

1.2: 1 h / 20 °C

2.1: phenyllithium / tetrahydrofuran / -78 °C

2.2: 20 °C

With sodium hydride; phenyllithium; In tetrahydrofuran; N,N-dimethyl-formamide;