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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766297Generated: November 4, 2026

Pyridine → HCID 11187117, compound

https://huagongshe.com/reaction/1766297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-2-methylbenzenesulfonyl chlorideHCID 522734—
Reactant6-Quinoxalinamine,2-methyl-(9CI)HCID 12666714—
SolventDichloromethaneHCID 6344—
ProductHCID 11187117HCID 1118711792.6%

Reaction Steps

To a solution of 3-chloro-2-methylbenzenesulphonyl chloride (119 mg, 0.528 mmol) in dichloromethane (3 mL) was added pyridine (100 μL, 1.26 mmol) and the mixture was stirred under N2 for 5 min, after which time 6-amino-2-methylquinoxaline (80 mg, 0.50 mmol) was added. The resulting mixture was stirred for 5 h. at room temperature, then saturated NaHCO3 solution (8 mL) was added 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 (161 mg, 92%), single spot at Rf 0.67 (ethyl acetate). mp 158.7-159.3° C., HPLC purity 99+% (tR 2.23 min in 10% water-acetonitrile). 1H NMR (CDCl3): δ 8.66 (1H, s), 8.02 (1H, d, J=7.7 Hz), 7.89 (1H, d, J=8.9 Hz), 7.61 (1H, d, J=2.5 Hz), 7.55 (1H, d, J=8.2 Hz), 7.46 (11H, dd, J=8.9, 2.5 Hz), 7.23 (1H, t, J=7.9 Hz), 7.08 (1H, s, N—H), 2.76 (3H, s), 2.71 (3H, s). LCMS: 346.11 (M−). FAB-MS (MH+, C16H14ClN3O2S): calcd 348.0573, found 348.0589.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230020B2
Source datasetuspto-grants-2007_06
ORD IDord-d5f6920034024be3ac5c32dae89dcb40
Source noteuspto-grants-2007_06