1H-Pyrazole-3-carboxylic acid, 5-[2-(4-chlorophenyl)-1-phenylethenyl]-1-[4-[[[[(4-methylphenyl)amino]thi oxomethyl]amino]sulfonyl]phenyl]-, ethyl ester

Base Information

Chemical Name:1H-Pyrazole-3-carboxylic acid, 5-[2-(4-chlorophenyl)-1-phenylethenyl]-1-[4-[[[[(4-methylphenyl)amino]thi oxomethyl]amino]sulfonyl]phenyl]-, ethyl ester
CAS No.:88289-97-8
Molecular Formula:C34H29ClN4O4S2
Molecular Weight:657.214
Hs Code.:

1H-Pyrazole-3-carboxylic acid,
5-[2-(4-chlorophenyl)-1-phenylethenyl]-1-[4-[[[[(4-methylphenyl)amino]thi
oxomethyl]amino]sulfonyl]phenyl]-, ethyl ester

Synonyms:

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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 1H-Pyrazole-3-carboxylic acid, 5-[2-(4-chlorophenyl)-1-phenylethenyl]-1-[4-[[[[(4-methylphenyl)amino]thi oxomethyl]amino]sulfonyl]phenyl]-, ethyl ester

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Technology Process of 1H-Pyrazole-3-carboxylic acid, 5-[2-(4-chlorophenyl)-1-phenylethenyl]-1-[4-[[[[(4-methylphenyl)amino]thi oxomethyl]amino]sulfonyl]phenyl]-, ethyl ester

There total 3 articles about 1H-Pyrazole-3-carboxylic acid, 5-[2-(4-chlorophenyl)-1-phenylethenyl]-1-[4-[[[[(4-methylphenyl)amino]thi oxomethyl]amino]sulfonyl]phenyl]-, ethyl ester 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: 75.0%

: 622-59-3
1-isothiocyanato-4-methylbenzene

: 88289-68-3
1-(p-sulfamylphenyl)-3-ethoxycarbonyl-5-(α-phenyl-p-chlorostyryl)pyrazole

: 88289-97-8
C₃₄H₂₉ClN₄O₄S₂

Guidance literature:: With potassium carbonate; In acetone; for 10h; Heating;
DOI:10.1002/jps.2600720908

Reference yield:

: 4392-54-5
4-aminosulfonylphenylhydrazine

: 88289-97-8
C₃₄H₂₉ClN₄O₄S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / ethanol / 6 h / Heating

2: 75 percent / potassium carbonate / acetone / 10 h / Heating

With potassium carbonate; In ethanol; acetone;
DOI:10.1002/jps.2600720908

Reference yield:

: ethyl 2,4-dioxo-6-(p-chlorophenyl)-5-phenylhex-5-enoate

: 88289-97-8
C₃₄H₂₉ClN₄O₄S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / ethanol / 6 h / Heating

2: 75 percent / potassium carbonate / acetone / 10 h / Heating

With potassium carbonate; In ethanol; acetone;
DOI:10.1002/jps.2600720908