2-Pyridinesulfonamide(6CI,7CI,9CI) Chemical Properties

Melting point:

140-141 °C(Solv: ethanol (64-17-5); water (7732-18-5))

Boiling point:

357.7±34.0 °C(Predicted)

Density 

1.417±0.06 g/cm3(Predicted)

storage temp. 

Inert atmosphere,Room Temperature

pka

9.21±0.60(Predicted)

Appearance

White to off-white Solid

InChI

InChI=1S/C5H6N2O2S/c6-10(8,9)5-3-1-2-4-7-5/h1-4H,(H2,6,8,9)

InChIKey

DWJMBQYORXLGAE-UHFFFAOYSA-N

SMILES

C1(S(N)(=O)=O)=NC=CC=C1

2-Pyridinesulfonamide(6CI,7CI,9CI) Usage And Synthesis

Synthesis

General procedure for the synthesis of pyridine-2-sulfonamide from 2-pyridinethione: To a 1000 mL round-bottomed flask was added dichloromethane (200 mL) and 1 M aqueous hydrochloric acid solution (200 mL, 200 mmol, 5.0 equiv.), and the suspension was cooled to -5 to -10 °C using an ice-salt bath. To the well-stirred suspension was added 2-mercaptopyridine (4.45 g, 40 mmol), and the resulting yellow mixture was stirred for 10 minutes, followed by the dropwise addition of 6% sodium hypochlorite solution (208 mL, 132 mmol, 3.3 eq.) over 5 minutes. After the dropwise addition, the mixture was continued to be stirred at the same temperature for 10 min and subsequently transferred to a separatory funnel for separation. The separated organic layer was immediately added dropwise to a pre-cooled and stirred mixture of saturated ammonia methanol solution (80 mL) and dichloromethane (80 mL) at 0 °C. The aqueous layer in the partition funnel was washed twice with dichloromethane, and the organic layer was combined and added dropwise to the ammonia solution. The resulting white suspension was slowly warmed to room temperature and stirred for 2 hours. Subsequently, the solvent was removed by evaporation to give a white solid. The solid was dissolved in hot ethyl acetate (250 mL x 2) and filtered through filter paper to remove ammonium chloride. The filtrate was evaporated to give the crude product, which was finally purified by recrystallization from ethyl acetate and hexane to give pure pyridine-2-sulfonamide (4.15 g, 70% yield). The product was characterized by 1H NMR (500 MHz, DMSO-d6) and 13C NMR (125 MHz, DMSO-d6) and the data were consistent with the expected structure.

References

[1] Angewandte Chemie - International Edition, 2008, vol. 47, # 47, p. 9125 - 9129
[2] Synlett, 2018, vol. 29, # 9, p. 1232 - 1238
[3] Patent: WO2016/131098, 2016, A1. Location in patent: Page/Page column 122; 123
[4] Acta Poloniae Pharmaceutica, 1955, vol. 12, p. 5,8
[5] Chem.Abstr., 1957, p. 17911

2-Pyridinesulfonamide(6CI,7CI,9CI)(63636-89-5)Related Product Information

• Pyridine hydrochloride
• 2,6-Pyridinedicarbonitrile
• 4-Pyridinesulfonamide(6CI,9CI)
• 2,3,5,6-Tetraaminopyridine trihydrochloride
• Pyridine trifluoroacetate
• PYRIDINE-2-THIOAMIDE
• dimethyl pyridine-3,5-dicarboxylate
• METHYL ISONICOTINATE
• Pyridine-N-oxide
• 2-Pyridinecarbaldehyde oxime
• PYRIDINE-2-SULFONYL FLUORIDE
• PYRIDINE-3,4-DICARBOXYLIC ANHYDRIDE
• PYRIDINE-2-SULFONYL CHLORIDE
• Pyridine-2-sulfonic acid cyclopropylaMide
• pyridine-4-sulfonyl fluoride
• Pyridine-2-sulfonic acid methylamide
• Pyridine-2-sulfonic acid tert-butylamide
• Pyridine-4-sulfonic acid methylamide