3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Base Information

Chemical Name:3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide
CAS No.:1232985-58-8
Molecular Formula:C₁₇H₁₅Cl₂N₃OS
Molecular Weight:380.298
Hs Code.:

Synonyms:3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-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-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Chemical Property:

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Technology Process of 3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

There total 5 articles about 3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-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: 71.0%

: 1208986-03-1
(E)-1-(3,4-dichlorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one

: 79-19-6
thiosemicarbazide

: 1232985-58-8
3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Guidance literature:: With potassium hydroxide; In ethanol; Reflux;
DOI:10.2174/1570178617999201106113114

Reference yield:

: C₁₇H₁₅Cl₂N₃OS

: 1232985-58-8
3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Guidance literature:: With potassium hydroxide; In ethanol; Reflux;
DOI:10.1016/j.bmc.2012.09.021

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 1232985-58-8
3-(3,4-dichlorophenyl)-5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium hydroxide / ethanol; water / 0 - 20 °C

2: potassium hydroxide / ethanol; water / 20 °C

3: potassium hydroxide / ethanol / Reflux

4: potassium hydroxide / ethanol / Reflux

With potassium hydroxide; In ethanol; water;
DOI:10.1016/j.bmc.2012.09.021