ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate

Base Information

• Chemical Name: ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate
• CAS No.: 1383478-63-4
• Molecular Formula: C₂₀H₁₇N₇O₂S₂
• Molecular Weight: 451.533

Synonyms:ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate

Chemical Property of ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate

Chemical Property:

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Technology Process of ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate

There total 2 articles about ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate 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: 60.0%

4-[5-amino-4-cyano-3-(methylsulfanyl)-1H-pyrazol-1-yl]-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidine-5-carbonitrile (1383478-60-1) + orthoformic acid triethyl ester (122-51-0) → ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate (1383478-63-4)

Guidance literature:

In acetic anhydride; for 2h; Reflux;

DOI:10.1007/s11164-012-0597-7

Reference yield:

[Bis(methylthio)methylene]malononitrile (5147-80-8) → ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate (1383478-63-4)

Guidance literature:

Multi-step reaction with 2 steps

1: triethylamine / methanol / Reflux

2: acetic anhydride / 2 h / Reflux

With triethylamine; In methanol; acetic anhydride;

DOI:10.1007/s11164-012-0597-7

Reference yield: 75.0%

ethyl{4-cyano-1-[5-cyano-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidin-4-yl]-3-(methylsulfanyl)-1H-pyrazol-5-yl}imidoformate (1383478-63-4) → 4-[4-hydrazinyl-3-(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidine-5-carbonitrile (1383478-66-7)

Guidance literature:

With hydrazine hydrate; In methanol; for 8h;

DOI:10.1007/s11164-012-0597-7

upstream raw materials:

[Bis(methylthio)methylene]malononitrile

4-[5-amino-4-cyano-3-(methylsulfanyl)-1H-pyrazol-1-yl]-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidine-5-carbonitrile

orthoformic acid triethyl ester

Downstream raw materials:

4-[4-hydrazinyl-3-(methylsulfanyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-6-(2-methoxyphenyl)-2-thioxo-1,2-dihydropyrimidine-5-carbonitrile

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