1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

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Chemical Name:1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene
CAS No.:1307304-50-2
Molecular Formula:C₂₄H₂₈N₆
Molecular Weight:400.527
Hs Code.:

Synonyms:1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

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Chemical Property of 1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

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Technology Process of 1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

There total 3 articles about 1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene 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:

: 1307304-46-6
(2S,2'S)-tert-butyl 2,2'-(4,4'-(1E,1'E)-2,2'-(1,4-phenylene)bis(ethene-2,1-diyl)bis(1H-imidazole-4,2-diyl))dipyrrolidine-1-carboxylate

: 1307304-50-2
1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

Guidance literature:: (2S,2'S)-tert-butyl 2,2'-(4,4'-(1E,1'E)-2,2'-(1,4-phenylene)bis(ethene-2,1-diyl)bis(1H-imidazole-4,2-diyl))dipyrrolidine-1-carboxylate; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 4h;

With ammonia; In methanol; dichloromethane;

Reference yield:

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 1307304-50-2
1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / Inert atmosphere

2: ammonium acetate / toluene / Reflux

3: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

With ammonium acetate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; toluene; acetonitrile;

Reference yield:

: 1307304-45-5
(2S,2'S)-2',2-((3E,3'E)-4,4'-(1,4-phenylene)bis(2-oxobut-3-ene-4,1-diyl))1-tert-butyl dipyrrolidine-1,2-dicarboxylate

: 1307304-50-2
1-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-4-yl)vinyl)-4-((E)-2-(2-((S)-pyrrolidin-2-yl)-1H-imidazol-5-yl)vinyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium acetate / toluene / Reflux

2: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

With ammonium acetate; trifluoroacetic acid; In dichloromethane; toluene;