3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

Base Information

Chemical Name:3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide
CAS No.:1360145-41-0
Molecular Formula:C₂₃H₁₈ClN₃OS₂
Molecular Weight:452
Hs Code.:

Synonyms:3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

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Technology Process of 3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

There total 5 articles about 3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide 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: 72.0%

: 1360145-34-1
6-chloro-7-methyl-2-(4-(phenylthio)phenyl)-4H-chromen-4-one

: 4426-72-6,51433-48-8,57-56-7
hydrazine carboxamide

: 1360145-41-0
3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

Guidance literature:: With potassium hydroxide; In ethanol; water; at 65 ℃; for 0.933333h; Sonication;
DOI:10.1080/10426507.2011.610850

Reference yield:

: 1355360-73-4
(E)-1-(5-chloro-2-hydroxy-4-methylphenyl)-3-(4-(phenylthio)phenyl)prop-2-en-1-one

: 1360145-41-0
3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: iodine / dimethyl sulfoxide / 2 h / 120 °C

2: potassium hydroxide / ethanol; water / 0.93 h / 65 °C / Sonication

With iodine; potassium hydroxide; In ethanol; water; dimethyl sulfoxide;
DOI:10.1080/10426507.2011.610850

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 1360145-41-0
3-(5-chloro-2-hydroxy-4-methylphenyl)-5-(4-(phenylthio)phenyl)-1H-pyrazole-1-carbothioamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 120 °C

2: potassium hydroxide / ethanol; water / Sonication

3: iodine / dimethyl sulfoxide / 2 h / 120 °C

4: potassium hydroxide / ethanol; water / 0.93 h / 65 °C / Sonication

With iodine; potassium carbonate; potassium hydroxide; In ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 2: Claisen Schmidt condensation;
DOI:10.1080/10426507.2011.610850