(Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

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Chemical Name:(Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one
CAS No.:1415565-82-0
Molecular Formula:C₂₂H₁₇ClN₄O
Molecular Weight:388.856
Hs Code.:

Synonyms:(Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

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Chemical Property of (Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

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Technology Process of (Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

There total 3 articles about (Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one 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: 58.0%

: 1415565-87-5
3-(3-(1H-indol-5-yl)prop-2-ynylamino)-1-benzyl-5-chloropyrazin-2(1H)-one

: 1415565-82-0
(Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

Guidance literature:: With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; trifluoroacetic acid; In chloroform; at 20 ℃; regioselective reaction;
DOI:10.1016/j.tet.2012.10.019

Reference yield:

: 1415565-67-1
1-benzyl-5-chloro-3-(prop-2-ynylamino)pyrazin-2(1H)-one

: 1415565-82-0
(Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / dimethyl sulfoxide / 0.5 h / 45 °C / Inert atmosphere

2: trifluoroacetic acid; (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate / chloroform / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; triethylamine; trifluoroacetic acid; In chloroform; dimethyl sulfoxide; 1: |Sonogashira Cross-Coupling;
DOI:10.1016/j.tet.2012.10.019

Reference yield:

: 87486-35-9
1-benzyl-3,5-dichloro-1H-pyrazin-2-one

: 1415565-82-0
(Z)-3-((1H-indol-5-yl)methylene)-7-benzyl-5-chloro-2,3-dihydroimidazo[1,2-a]pyrazin-8(7H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 70 °C

2: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / dimethyl sulfoxide / 0.5 h / 45 °C / Inert atmosphere

3: trifluoroacetic acid; (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate / chloroform / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; chloroform; dimethyl sulfoxide; 2: |Sonogashira Cross-Coupling;
DOI:10.1016/j.tet.2012.10.019