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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513501Generated: October 26, 2026

Benzenesulfonyl chloride → N-[1,5]Naphthyridin-4-yl-benzenesulfonamide

https://huagongshe.com/reaction/513501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
Reactant1,5-Naphthyridin-4-amineHCID 589354—
SolventTetrahydrofuranHCID 8028—
ProductN-[1,5]Naphthyridin-4-yl-benzenesulfonamideHCID 6818335230%

Reaction Steps

[1,5]Naphthyridin-4-ylamine (Intermediate 486) (60 mg, 0.41 mmol) was added to a suspension of NaH (60% in mineral oil; 25 mg, 0.53 mmol) in THF (2 ml) at 0° C. followed by a solution of benzenesulfonyl chloride (95 mg, 0.53 mmol) in THF (1 ml). The mixture was stirred at room temperature for 12 h. After completion, the reaction was quenched with water (5 ml) and the aqueous phase was extracted with EtOAc (30 ml). The organic phase was washed with brine, dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with DCM/MeOH (98:2) as the eluent to give the title compound (30 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102688B2
Source datasetuspto-grants-2015_08
ORD IDord-c23348d195094824a5494dead84175ca
Source noteuspto-grants-2015_08