Production Method 1

223463-13-6

874959-68-9

Reaction Conditions

1.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ;  15 min, 0 °C
1.2 3 h, 25 °C
1.3 Solvents: Water ;  cooled
2.1 Reagents: Sulfuryl chloride Solvents: Dichloromethane ;  0 °C → rt; 30 min, rt

Reference

2-Phenylindole and arylsulfonamide: novel scaffolds bactericidal against Mycobacterium tuberculosis

Naik, Maruti; et al, ACS Medicinal Chemistry Letters, 2014, 5(9), 1005-1009

5-Bromopyridine-2-sulfonyl chloride Raw materials

• 5-Bromo-2-iodopyridine

5-Bromopyridine-2-sulfonyl chloride Preparation Products

• 5-Bromopyridine-2-sulfonyl chloride (874959-68-9)

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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridines and derivatives
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives

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