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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766290Generated: November 1, 2026

Pyridine → HCID 11462138, compound

https://huagongshe.com/reaction/1766290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Methylquinolin-6-amineHCID 103148—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-2-methylbenzenesulfonyl chlorideHCID 522734—
SolventDichloromethaneHCID 6344—
ProductHCID 11462138HCID 1146213868%

Reaction Steps

To a solution of 3-chloro-2-methylbenzenesulphonyl chloride (149 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 90 min 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 (148 mg, 68%), single spot at Rf 0.64 (ethyl acetate). mp 178.1-178.4° C., HPLC purity 99+% (tR 2.27 min in 10% water-acetonitrile). 1H NMR (CDCl3): δ 7.93-7.89 (3H, m), 7.53 (1H, d, J=8.2 Hz), 7.44 (1H, d, J=2.5 Hz), 7.31-7.24 (2H, m), 7.18 (1H, t, J=8.1 Hz), 2.73 (3H, s), 2.69 (3H, s). LCMS: 345.17 (M−). FAB-MS (MH+, C17H15CIN2O2S): calcd 347.0621, found 347.0622.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230020B2
Source datasetuspto-grants-2007_06
ORD IDord-03f2a811b6c04fa1b1d8998fca62e668
Source noteuspto-grants-2007_06