Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766292Generated: November 4, 2026

Pyridine → HCID 11280072, compound

https://huagongshe.com/reaction/1766292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,5-Dichlorobenzenesulfonyl chlorideHCID 79401—
Reactant2-Methylquinolin-6-amineHCID 103148—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductHCID 11280072HCID 1128007252%

Reaction Steps

To a solution of 2,5-dichlorobenzenesulphonyl chloride (163 mg, 0.664 mmol) in dichloromethane (4 mL) was added pyridine (130 μL, 1.58 mmol) and the mixture was stirred under N2 for 5 min, after which time 6-amino-2-methylquinoline (100 mg, 0.632 mmol) was added. The resulting mixture was stirred for 2 h at room temperature, then saturated NaHCO3 solution (10 mL) was added and the mixture was extracted into ethyl acetate (20 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 an off-white solid (120 mg, 52%), single spot at Rf 0.68 (ethyl acetate). mp 124.6-125.0° C., HPLC purity 99+% (tR 2.22 min in 10% water-acetonitrile). 1H NMR (CDCl3): δ 7.98 (1H, d, 2.2 Hz), 7.94 (1H, d, J=8.4 Hz), 7.88 (1H, d, J=8.9 Hz), 7.57 (1H, d, J=2.2 Hz), 7.45-7.35 (3H, m), 7.27-7.24 (2H, m), 2.68 (3H, s). LCMS: 365.10 (M−). FAB-MS (MH+, C16H12Cl2N2O2S): calcd 367.0075, found 367.0074.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230020B2
Source datasetuspto-grants-2007_06
ORD IDord-f0916729e72a4e6bb5c7878e34a8d301
Source noteuspto-grants-2007_06