3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Base Information

Chemical Name:3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide
CAS No.:1424400-73-6
Molecular Formula:C₂₀H₁₆ClN₃S
Molecular Weight:365.886
Hs Code.:

Synonyms:3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Suppliers and Price of 3-(4-chlorophenyl)-5-(naphthalen-1-yl)-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-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

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Technology Process of 3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

There total 4 articles about 3-(4-chlorophenyl)-5-(naphthalen-1-yl)-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: 79.0%

: 1-(4-chlorophenyl)-3-(1-naphthalenyl)prop-2-en-1-one

: 79-19-6
thiosemicarbazide

: 1424400-73-6
3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Guidance literature:: In ethanol; at 80 ℃; for 5h;
DOI:10.1016/j.bmc.2013.01.013

Reference yield:

: 56412-56-7
1-(4-chlorophenyl)-3-(naphthalen-1-yl)-2-propen-1-one

: 79-19-6
thiosemicarbazide

: 1424400-73-6
3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Guidance literature:: With potassium hydroxide; In ethanol; for 12h; Reflux;
DOI:10.1016/j.bmcl.2014.03.072

Reference yield:

: 66-77-3
1-naphthaldehyde

: 1424400-73-6
3-(4-chlorophenyl)-5-(naphthalen-1-yl)-4,5-dihydro-1H-pyrazole-1-carbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / Reflux

2: ethanol / 5 h / 80 °C

With sodium hydroxide; In ethanol;
DOI:10.1016/j.bmc.2013.01.013