Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Picolinic acid | HCID 1018 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 4-(tert-butyl)-N-[3-(2-hydroxyethoxy)-1-methyl-4-(4-methylphenyl)-1H-pyrazol-5-yl]benzenesulfonamide | HCID 22282043 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22282035 | HCID 22282035 | — |
Reaction Steps
2-Pyridine carboxylic acid (278 mg) and triethylamine (0.321 ml) in toluene (10 ml) was stirred under nitrogen at room temperature for 10 mins. Diphenyl phosphoryl azide (621 mg) was added to the reaction and warmed to 35-40° C. for 1 hour and then at 100° C. until the effervescence had ceased. 4-(tert-butyl)-N-[3-(2-hydroxyethoxy)-1-methyl-4-(4-methylphenyl)-1H-pyrazol-5-yl]benzenesulfonamide (200 mg) (Example 2) and 4-dimethylaminopyridine (8 mg) in toluene (5 ml) was added to the reaction and stirred at 100° C. for a further 45 minutes. The reaction was quenched with water (2 ml) and left to cool. The crude product was loaded onto silica (25 g) and eluted with a solvent gradient of pentane:ethyl acetate (1:0 to 0:1) to yield the title compound as a white solid (106 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06962923B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-dcdd9df6b4104cba832506f0b894e22c |
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| Source note | uspto-grants-2005_11 |
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