HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742063Generated: November 3, 2026
4-Toluenesulfonyl chloride → 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole
https://huagongshe.com/reaction/1742063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole | HCID 73508416 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole | HCID 73508419 | 73.1% |
Reaction Steps
7.4 g (0.028 mol) of 5-amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole are treated in 90 ml of absolute acetonitrile with 4 ml (0.028 mol) of triethylamine and then, with stirring at room temperature, are treated dropwise with a solution of 5.55 g (0.029 mol) of 4-tosyl chloride in 150 ml of absolute acetonitrile. Stirring is continued for 1 hour and then the mixture is evaporated to dryness. The residue is treated with water and ethyl acetate, the organic phase is washed with water, dried over magnesium sulphate and evaporated under vacuum. The oily residue obtained in this way is crystallised from ethanol. 8.5 g (72%) of 5-amino-3-methyl-1-(O-tosyl-3-nitrobenzohydroximoyl)-pyrazole with a m. pt. of 156°-158° C. are obtained. The substance is light-sensitive. On recrystallising twice from ethanol, the m. pt. is 165°-169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05336780 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-9e7aea21da4748b6b736179a167e9b9f |
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| Source note | uspto-grants-1994_08 |
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