HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103872Generated: October 27, 2026
4-(hydrazinocarbonyl)-N-methylbenzenesulfonamide → 4-({2-[[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl](phenyl)methylene]hydrazino}carbonyl)-N-methylbenzenesulfonamide
https://huagongshe.com/reaction/2103872
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(hydrazinocarbonyl)-N-methylbenzenesulfonamide | HCID 67050214 | — |
| Reactant | [5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl](phenyl)methanone | HCID 67050263 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-({2-[[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl](phenyl)methylene]hydrazino}carbonyl)-N-methylbenzenesulfonamide | HCID 72359991 | 22% |
Reaction Steps
[5-(4-t-Butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl] (phenyl)methanone (0.254 mmol, 85 mg), 4-(hydrazinocarbonyl)-N-methylbenzenesulfonamide (0.254 mmol, 58 mg) and p-tosylic acid monohydrate (30 mol %, 13 mg) were dissolved in isopropyl alcohol (8.5 mL) and stirred at 100° C. for 19 hours. Then, the solvent was evaporated, and the residue was purified by silica gel thin layer chromatography (chloroform/methanol=10/1) to give the desired product as a yellow solid (30.3 mg, yield 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576115B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-59d181443d5c46c68677439ffb26da26 |
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| Source note | uspto-grants-2009_08 |
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