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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507361Generated: October 25, 2026

Pyridine → 2,5-dichloro-N-(2-methyl-benzooxazol-5-yl)-benzenesulfonamide

https://huagongshe.com/reaction/507361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,5-Dichlorobenzenesulfonyl chlorideHCID 79401—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Methyl-1,3-benzoxazol-5-amineHCID 737920—
SolventDichloromethaneHCID 6344—
Product2,5-dichloro-N-(2-methyl-benzooxazol-5-yl)-benzenesulfonamideHCID 2534834763%

Reaction Steps

To a solution of 2,5-dichlorobenzenesulphonyl chloride (52 mg, 0.21 mmol) in dichloromethane (1.5 mL) was added pyridine (40 μL, 0.5 mmol) and the mixture was stirred under N2 for 5 min, after which time 5-amino-2-methylbenzoxazole (30 mg, 0.20 mmol) was added. The resulting mixture was stirred for 1 h at room temperature, then saturated NaHCO3 solution was added (8 mL) and the mixture was extracted into ethyl acetate (15 mL). The organic phase was washed with brine, dried (Na2SO4), filtered and evaporated to give a residue that was purified using flash chromatography to afford a pale pink solid (45 mg, 63%), single spot at Rf 0.53 (1:1 hexane:ethyl acetate). mp 193.5-193.9° C., HPLC purity 98% (tR 2.27 min in 10% water-acetonitrile). 1H NMR (CDCl3): δ 7.86 (1H, d, J=2.2 Hz), 7.39 (4H, m), 7.12 (1H, dd, J=8.4, 1.8 Hz), 2.58 (3H, s). LCMS: 355.07 (M−). FAB-MS (MH+, C14H10Cl2N2O3S): calcd 356.9867, found 356.9878.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786152B2
Source datasetuspto-grants-2010_08
ORD IDord-701cfdddfb2c4991b7841819602d7f7b
Source noteuspto-grants-2010_08