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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methyl-1,3-benzoxazol-5-amine | HCID 737920 | — |
| Reactant | 4-N-Propylbenzenesulphonyl chloride | HCID 2737222 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-methyl-benzooxazol-5-yl)-4-propyl-benzenesulfonamide | HCID 11724187 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07309715B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-3df574cc829340469b0b4aefc808826a |
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| Source note | uspto-grants-2007_12 |
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