phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

Base Information

Chemical Name:phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate
CAS No.:1414568-64-1
Molecular Formula:C₁₈H₁₅N₃O₃S
Molecular Weight:353.401
Hs Code.:

Synonyms:phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

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Chemical Property of phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

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Technology Process of phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

There total 4 articles about phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate 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:

: 1414568-68-5
phenyl 2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-ylcarbamate

: 1414568-64-1
phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; at -50 ℃; for 1h;

Reference yield:

: 1885-14-9
phenyl chloroformate

: 1414568-64-1
phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethyl acetate; water / 17 h / 20 °C

2: 3-chloro-benzenecarboperoxoic acid / tetrahydrofuran / 1 h / -50 °C

With 3-chloro-benzenecarboperoxoic acid; sodium hydroxide; In tetrahydrofuran; water; ethyl acetate;

Reference yield:

: 16563-14-7
4-oxotetrahydrothiophene-3-carbonitrile

: 1414568-64-1
phenyl (5-oxido-2-phenyl-4,6-dihydro-2H-thieno[3,4-c]pyrazol-3-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 2 h / Reflux

2: sodium hydroxide / ethyl acetate; water / 17 h / 20 °C

3: 3-chloro-benzenecarboperoxoic acid / tetrahydrofuran / 1 h / -50 °C

With 3-chloro-benzenecarboperoxoic acid; sodium hydroxide; In tetrahydrofuran; ethanol; water; ethyl acetate;