HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744590Generated: October 26, 2026
Diisopropyl Ether → N-{3-Cyano-4-[bis(2-hydroxyethyl)amino]phenyl}-1-(4-fluorophenyl)-5-methylpyrazole-4-carboxamide
https://huagongshe.com/reaction/1744590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-(4-fluorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acid | HCID 4270263 | — |
| Reactant | 5-Amino-2-[bis(2-hydroxyethyl)amino]benzonitrile | HCID 21942366 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-{3-Cyano-4-[bis(2-hydroxyethyl)amino]phenyl}-1-(4-fluorophenyl)-5-methylpyrazole-4-carboxamide | HCID 22228135 | 23.5% |
Reaction Steps
1-(4-Fluorophenyl)-5-methylpyrazole-4-carboxylic acid (2.0 g), 5-amino-2-[bis(2-hydroxyethyl)amino]benzonitrile (2.0 g), 1-hydroxybenzotriazole (1.5 g) and 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide (2.0 g) were added to dimethylformamide (25 ml) and the mixture was stirred at room temperature for 5 h. The reaction mixture was treated with aqueous potassium carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (mobile phase:chloroform:methanol=100:1) to give an oily substance. Diisopropyl ether was added to the oily substance to allow crystallization. The crystals were recrystallized from a mixed solvent of ethyl acetate-diisopropyl ether to give the title compound (0.9 g), melting point: 158–159° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07015218B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-b23b30eca8e84383b593e4405449c898 |
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| Source note | uspto-grants-2006_03 |
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