ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate

Base Information

Chemical Name:ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate
CAS No.:139346-63-7
Molecular Formula:C₂₉H₂₈N₂O₅S
Molecular Weight:516.618
Hs Code.:

Synonyms:ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate

There total 1 articles about ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate 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:

: 117376-95-1
3-phenyl-7-(2-phenyl-2-oxoethyl)-5,6-dihydroimidazo<2,1-b>thiazolium bromide

: 623-47-2
propynoic acid ethyl ester

: 139346-63-7
ethyl (2Z,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate

: 139313-20-5
ethyl (2E,5Z)-6-<5-benzoyl-2,3-dihydro-7-(ethoxycarbonyl)-1H-pyrrolo<1,2-a>imidazol-1-yl>-6-phenyl-4-thiahexa-2,5-dienoate

Guidance literature:: With triethylamine; In acetonitrile; at 20 ℃; for 2h; Product distribution; temperature and solvent effects;
DOI:10.1021/jo00034a029