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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036549Generated: October 30, 2026

Hydrochloric Acid → HCID 57870807, compound

https://huagongshe.com/reaction/1036549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-3-(trifluoromethyl)benzenesulfonyl ChlorideHCID 2780719—
Reactant3-Amino-5-methylpyridine-2-carbonitrileHCID 53395375—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57870807HCID 5787080788%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 3-amino-5-methylpicolinonitrile (9.6 g, 72 mmol) in pyridine (63 mL) was added 4-chloro-3-trifluoromethyl-benzenesulfonyl chloride (19.6 g, 80 mmol) in one portion and the resulting reaction mixture was stirred at 60° C. for overnight. Pyridine was removed in vacuo, added 2N HCl (100 mL), extracted with EtOAc (3×300 mL; Note: due to the amide presence, solubility in EtOAc is low). Combined EtOAc layers were dried (Na2SO4), evaporated to obtain 26.3 g of crude product which contained a small amount of bis-sulfonamide which was subjected to hydrolysis in THF (200 mL) with 2N NaOH (100 mL) at room temperature for 2 hours. 2 N HCl (100 mL) Was added, extracted with EtOAc (1×700 mL, 1×250 mL), combined EtOAc layers were washed with saturated NaHCO3 solution (2×250 mL), dried (Na2SO4) and evaporated to obtain 22 g of monosulfonamide. To this dioxane (350 mL), water (450 mL) (Note: requires high dilution for fast reaction) was added, followed by NaOH (30 g, 0.75 mol) and stirred under reflux for 24 hours. Dioxane was removed in vacuo and conc. HCl (75 mL) was added slowly with cooling. The resultant solid was filtered, washed with water and dried in vacuo to afford title compound (22 g, 88% for 2 steps) as light yellow solid. (M+H) Expected: 395.0; found 394.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546408B2
Source datasetuspto-grants-2013_10
ORD IDord-d85e63e23cfd4adb9ca5649f29ce7e28
Source noteuspto-grants-2013_10