2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

Base Information

Chemical Name:2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid
CAS No.:1264296-68-5
Molecular Formula:C₂₂H₁₈ClN₃O₂
Molecular Weight:391.857
Hs Code.:

Synonyms:2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

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Chemical Property of 2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

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Technology Process of 2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

There total 4 articles about 2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid 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:

: C₂₆H₂₆ClN₃O₂

: 1264296-68-5
2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

Guidance literature:: With trifluoroacetic acid; In acetonitrile; at 20 ℃; for 12h;

Reference yield:

: 39149-65-0
tert-butyl 2-methyl-3-oxobutanoate

: 1264296-68-5
2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 3 h / 100 °C

2: trifluoroacetic acid / tert-butyl alcohol / 1 h / 60 °C

3: caesium carbonate / acetonitrile / 3 h / 80 °C

4: trifluoroacetic acid / acetonitrile / 12 h / 20 °C

With caesium carbonate; trifluoroacetic acid; In acetonitrile; tert-butyl alcohol;

Reference yield:

: 1264296-66-3
C₁₂H₂₁NO₃

: 1264296-68-5
2-(3-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidin-7-yl)-2-methyl-3-phenylpropanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / tert-butyl alcohol / 1 h / 60 °C

2: caesium carbonate / acetonitrile / 3 h / 80 °C

3: trifluoroacetic acid / acetonitrile / 12 h / 20 °C

With caesium carbonate; trifluoroacetic acid; In acetonitrile; tert-butyl alcohol;