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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970044Generated: October 25, 2026

Pyridine → N-(2-methyl-benzooxazol-5-yl)-4-propyl-benzenesulfonamide

https://huagongshe.com/reaction/970044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Methyl-1,3-benzoxazol-5-amineHCID 737920—
Reactant4-N-Propylbenzenesulphonyl chlorideHCID 2737222—
SolventDichloromethaneHCID 6344—
ProductN-(2-methyl-benzooxazol-5-yl)-4-propyl-benzenesulfonamideHCID 1172418785%

Reaction Steps

To a solution of 4n-propylbenzenesulphonyl chloride (93 mg, 0.43 mmol) in dichloromethane (2 mL) was added pyridine (80 μL, 1.0 mmol) and the mixture was stirred under N2 for 5 min, after which time 5-amino-2-methylbenzoxazole (60 mg, 0.40 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 oil (112 mg, 85%), single spot at Rf 0.53 (1:1 hexane:ethyl acetate). HPLC purity 99+% (tR 2.38 min in 10% water-acetonitrile) 1H NMR (CDCl3): δ 7.64 (2H, dt, J=8.1, 1.8 Hz), 7.31 (2H, m), 7.18 (2H, d, J=8.4 Hz), 7.06 (1H, dd, J=8.6, 2.4 Hz), 2.59 (5H, m), 1.58 (2H, sextet, J=7.3 Hz), 0.89 (3H, t, J=7.3 Hz). LCMS: 329.15 (M−). FAB-MS (MH+, C17H18N2O3S): calcd 331.1116, found 331.1118.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07309715B2
Source datasetuspto-grants-2007_12
ORD IDord-3df574cc829340469b0b4aefc808826a
Source noteuspto-grants-2007_12