HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860524Generated: November 3, 2026
Diisopropylethylamine → N-Phenyl-4-[1-phenyl-5-[(phenylsulfonyl)amino]-1H-pyrazol-3-yl]benzamide
https://huagongshe.com/reaction/1860524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 4-(5-benzenesulfonylamino-1-phenyl-1H-pyrazole-3-yl)-benzoic acid | HCID 69831010 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Phenyl-4-[1-phenyl-5-[(phenylsulfonyl)amino]-1H-pyrazol-3-yl]benzamide | HCID 12018686 | — |
Reaction Steps
Benzotriazol-1-yloxytripyrrolid inophosphonium hexafluorophosphate (0.136 g, 0.26 mmol) was added to a solution of 4-(5-benzenesulfonylamino-1-phenyl-1H-pyrazole-3-yl)-benzoic acid (0.10 g, 0.24 mmol) and N,N-diisopropylethylamine (0.062 ml, 0.36 mmol) in N,N-dimethylformamide (2 ml). 1-Hydroxybenzotriazole hydrate (30 mg, 0.24 mmol) and 4-(N,N-dimethylamino)pyridine (catalytic) were added and the resulting solution was stirred at room temperature for 3 hours. Water (7 ml) was added, and a precipitate was collected by filtration and washed with water. The solid was purified by preparative thin layer silica gel chromatography, using 2% methanol in dichloromethane as the eluant, to yield N-Phenyl-4-[1-phenyl-5-[(phenylsulfonyl)amino]-1H-pyrazol-3-yl]benzamide as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531478B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-03e0f0edbacd4ac6b245c68962c0e973 |
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| Source note | uspto-grants-2003_03 |
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