6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester

Base Information

Chemical Name:6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester
CAS No.:129095-24-5
Molecular Formula:C₂₆H₃₀N₄O₄
Molecular Weight:462.549
Hs Code.:

Synonyms:6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester

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Chemical Property of 6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester

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Technology Process of 6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester

There total 2 articles about 6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester 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: 84.0%

: 2969-81-5
Ethyl 4-bromobutyrate

: 129095-32-5
6-cyclohexyl-4,7-dihydro-2-phenyl-5H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8(6H)-dione

: 129095-24-5
6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester

Guidance literature:: With potassium carbonate; In dimethyl sulfoxide; at 50 ℃; for 17h;
DOI:10.1021/jm00109a028

Reference yield:

: 4563-90-0
4-Ethoxycarbonyl-1-cyclohexyl-3-hydroxy-3-pyrrolin-2-on

: 129095-24-5
6-cyclohexyl-5,6,7,8-tetrahydro-5,8-dioxo-2-phenyl-4H-pyrazolo<1,5-a>pyrrolo<3,4-d>pyrimidine-4-butanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / glacial acetic acid / Heating

2: 84 percent / K₂CO₃ / dimethylsulfoxide / 17 h / 50 °C

With potassium carbonate; acetic acid; In dimethyl sulfoxide;
DOI:10.1021/jm00109a028