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72811-73-5

72811-73-5 Structure

72811-73-5 Structure
IdentificationMore
[Name]

4-(3'-Methylphenyl)amino-3-pyridinesulfonamide
[CAS]

72811-73-5
[Synonyms]

3-SULFONAMIDO-4-(3-METHYLANILINO)-PYRIDINE
4-(-3-METHYLPHENYL)AMINO-3-PYRIDINESULFONAMIDE
4-(3'-METHYLPHENYL)AMINO-3-PYRIDINESULFONAMIDE
SPECS AJ-333/25006115
4-(3-METHYLPHENYL)AMINO-3-PYRIDINESULFONAMIDE (SMPAP)
4-[3-Methyl phenyl] amino-3-pyridine sulphonamide
Torasemide intermediate
[4-(3-Methylphenyl)amino]pyrid
4-(3-methylphenyl)amino-3-pyridine sulfonamide (intermediate of torasemide)
4-(3-methylphenylamino) Pyridine-3-sulfonamide
[4-3-Methylphenyl)amino]pyridine-3-sulphonamide
4-(3-METHYLPHENYL)AMINO-3-PYRIDINESULFONAMIDE 98%
[EINECS(EC#)]

615-805-8
[Molecular Formula]

C12H13N3O2S
[MDL Number]

MFCD00661332
[Molecular Weight]

263.32
[MOL File]

72811-73-5.mol
Chemical PropertiesBack Directory
[Melting point ]

162-164?C
[Boiling point ]

475.8±55.0 °C(Predicted)
[density ]

1.357±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

neat
[pka]

9.53±0.60(Predicted)
[color ]

White to Off-White
[BRN ]

5438165
[Major Application]

pharmaceutical (small molecule)
[InChI]

InChI=1S/C12H13N3O2S/c1-9-3-2-4-10(7-9)15-11-5-6-14-8-12(11)18(13,16)17/h2-8H,1H3,(H,14,15)(H2,13,16,17)
[InChIKey]

ZXPCUGWAKUIOOF-UHFFFAOYSA-N
[SMILES]

C1=NC=CC(NC2=CC=CC(C)=C2)=C1S(N)(=O)=O
[CAS DataBase Reference]

72811-73-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

WGK 3
[REACH Registrations]

Active
[HS Code ]

2935909550
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Hazard InformationBack Directory
[Chemical Properties]

White to Off-White Solid
[Uses]

Torasemide intermediate.
[Synthesis]

4-(3'-Methylphenyl)amino-3-pyridinesulfonamide is prepared by the reaction of 4-Chloropyridine-3-sulfonamide hydrochloride and 3-Methylaniline. The specific synthesis steps are as follows:
EXAMPLE 1; Preparation of 4-(3-methylphenyl)aminopyridine-sulfonamide; 2L three-neck flask, equipped with a mechanical stirrer, thermometer and condenser, was charged with water (500 ml) and 4-chloro-3- pyridinesulfonamide hydrochloride (100g, 0.44 mol). To this suspension was added m-toluidine (49.2 ml, 0.46 mol) at room temperature. The reaction mixture was heated to 90°C for a minimum period of 3 h. The progress of the reaction was followed by HPLC. After completion, the mixture was cooled to room temperature. The pH of the reaction was then adjusted carefully to pH 7-8 with sat. NaHC03 (ca. 1.1 l). The product was precipitated out and isolated by vacuum filtration as beige solid (126.2 g wet weight). The product was then dissolved in MeOH (1.0 l) at room temperature and charged with Darco KB (25g). The solution was refluxed for 0.5 h and then filtered through a patch of celite to remove Darco KB, while still hot, and rinsed with hot MeOH (200 ML). The filtrate was then charged with water (1.2 l) and stirred for a minimum of 1 h at room temperature. The product, which had precipitated out, was isolated by vacuum filtration to obtain a solid 106.3 g (92percent wet weight =>99.8percent purity a/a). 1H NMR (d6-DMSO) ; 2.30 (s, 3H), 7.00-7. 15 (m. 5H), 7.32 (m, 1H), 7.75 (brs, 1.5H), 8.05 (brs, 0.5H), 8.25 (d, 1H), 8.68 (s, 1H).
4-(3'-Methylphenyl)amino-3-pyridinesulfonamide synthesis
[References]

[1] Patent: WO2004/89904, 2004, A2. Location in patent: Page 7
Spectrum DetailBack Directory
[Spectrum Detail]

4-(3'-Methylphenyl)amino-3-pyridinesulfonamide(72811-73-5)1HNMR
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