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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173141Generated: October 31, 2026

4-Chlorobenzenesulfonyl chloride → HCID 17838655, compound

https://huagongshe.com/reaction/1173141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant1,6-Naphthyridin-2-amineHCID 589353—
SolventDichloromethaneHCID 6344—
ProductHCID 17838655HCID 1783865521.44%

Reaction Conditions

Temperature40 °C

Reaction Steps

2-Amino-1,6-naphthyridine (200 mg, Production Example 25b) was dissolved in dichloromethane (6.0 ml), to which were then added triethylamine (0.20 ml) and 4-chlorobenzenesulfonyl chloride (0.31 g), followed by stirring at 40° C. for 1.5 hours. An aqueous saturated sodium bicarbonate was added thereto, followed by extracting with ethyl acetate. The extract was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column, to give the title compound (84 mg, 21.44%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834049B2
Source datasetuspto-grants-2010_11
ORD IDord-ebe0bf55649d45c29fab50e142a0014b
Source noteuspto-grants-2010_11