HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016604Generated: October 27, 2026
Pyridine → 3-(4-chlorophenyl)-N-((4-chlorophenyl)sulfonyl)-4-phenyl4,5-dihydro-1H-pyrazole-1-carboxamide
https://huagongshe.com/reaction/1016604
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl (4-chlorophenyl)sulfonylcarbamate | HCID 5013687 | — |
| Reactant | 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole | HCID 11368884 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(4-chlorophenyl)-N-((4-chlorophenyl)sulfonyl)-4-phenyl4,5-dihydro-1H-pyrazole-1-carboxamide | HCID 11374894 | 83.4% |
Reaction Steps
Part A: To a solution of N-((4-chlorophenyl)sulfonyl)carbamic acid methyl ester (CAS: 34543-04-9) (2.99 gram, 12.0 mmol) and pyridine (4 ml) in 1,4-dioxane (20 ml) was added 3-(4-chlorophenyl)-4,5-dihydro-4-phenyl-1H-pyrazole (3.39 gram, 13.2 mmol) and the resulting mixture was stirred for 4 hours at 100° C. After concentration in vacuo the residue was dissolved in dichloromethane, successively washed with water, 1 N HCl and water, dried over anhydrous Na2SO4, filtered and concentrated in vacuo to a volume of 20 ml. Methyl-tert-butyl ether (60 ml) was added and the resulting solution was concentrated to a volume of 20 ml. The formed crystals were collected by filtration and recrystallised from methyl-tert-butyl ether to give 3-(4-chlorophenyl)-N-((4-chlorophenyl)sulfonyl)-4,5-dihydro-4-phenyl-1H-pyrazole-1-carboxamide (4.75 gram, 76% yield). Melting point: 211-214° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476060B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-0fde4bf5b2244b4580ef22aba542466e |
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| Source note | uspto-grants-2002_11 |
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