5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Base Information

Chemical Name:5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one
CAS No.:1370409-68-9
Molecular Formula:C₂₅H₂₈N₆O₄S
Molecular Weight:508.601
Hs Code.:

Synonyms:5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

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Chemical Property of 5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

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Technology Process of 5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

There total 2 articles about 5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-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:

: C₂₅H₃₀N₆O₅S

: 1370409-68-9
5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Guidance literature:: With sodium ethanolate; In ethanol; at 120 ℃; for 2h;
DOI:10.1016/j.bmcl.2012.01.119

Reference yield:

: 194602-23-8
2-Ethoxy-5-(4-methylpiperazin-1-ylsulphonyl)benzoic acid

: 1370409-68-9
5-(2-ethoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1-methyl-3-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: Imidazole hydrochloride / tetrahydrofuran / 4 h / 50 °C

2: tetrahydrofuran / 50 °C

3: sodium ethanolate / ethanol / 2 h / 120 °C

With sodium ethanolate; Imidazole hydrochloride; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmcl.2012.01.119