3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

Base Information

Chemical Name:3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate
CAS No.:144899-60-5
Molecular Formula:C₂₂H₁₇N₃OS
Molecular Weight:371.462
Hs Code.:

Synonyms:3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

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Chemical Property of 3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

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Technology Process of 3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

There total 3 articles about 3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate 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: 74.0%

: 103-72-0
phenyl isothiocyanate

: 145196-85-6
2-phenacyl-3,4-dihydropyrrolo<1,2-a>pyrazinium bromide

: 144899-60-5
3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

Guidance literature:: With potassium carbonate; In acetonitrile; for 24h; Ambient temperature;
DOI:10.1016/S0040-4020(01)89452-7

Reference yield:

: 29709-35-1
1-(2-aminoethyl)pyrrole

: 144899-60-5
3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

Guidance literature:: Multi-step reaction with 3 steps

1: 15 h / Heating

2: 63 percent / acetone / 4 h / Heating

3: 74 percent / K₂CO₃ / acetonitrile / 24 h / Ambient temperature

With potassium carbonate; In acetone; acetonitrile;
DOI:10.1016/S0040-4020(01)89452-7

Reference yield:

: 71257-37-9
3,4-dihydropyrrolo[1,2-a]-pyrazine

: 144899-60-5
3-benzoyl-1-phenyl-5,6-dihydroimidazo<1,2-a>pyrrolo<2,1-c>pyrazin-4-ium-2-thiolate

Guidance literature:: Multi-step reaction with 2 steps

1: 63 percent / acetone / 4 h / Heating

2: 74 percent / K₂CO₃ / acetonitrile / 24 h / Ambient temperature

With potassium carbonate; In acetone; acetonitrile;
DOI:10.1016/S0040-4020(01)89452-7