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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062746Generated: November 2, 2026

Picolinic acid → HCID 22282035, compound

https://huagongshe.com/reaction/1062746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-(tert-butyl)-N-[3-(2-hydroxyethoxy)-1-methyl-4-(4-methylphenyl)-1H-pyrazol-5-yl]benzenesulfonamideHCID 22282043—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
ProductHCID 22282035HCID 22282035—

Reaction Conditions

Temperature37.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962923B2
Source datasetuspto-grants-2005_11
ORD IDord-dcdd9df6b4104cba832506f0b894e22c
Source noteuspto-grants-2005_11