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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513963Generated: October 30, 2026

Methanesulfonyl chloride → 2-{7-[(3,4-Difluorophenyl)methoxy]-1,5-naphthyridin-3-yl}acetonitrile

https://huagongshe.com/reaction/513963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methanolHCID 86301659—
Reactant(7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methyl methanesulfonateHCID 90418375—
SolventDichloromethaneHCID 6344—
Product2-{7-[(3,4-Difluorophenyl)methoxy]-1,5-naphthyridin-3-yl}acetonitrileHCID 8630166064%

Reaction Steps

(7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methyl methanesulfonate. To a solution of (7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)methanol (Example 73, 90 mg, 0.3 mmol) in DCM (4 mL) was added methanesulfonyl chloride (0.05 mL, 0.61 mmol) followed by TEA (0.06 mL, 0.43 mmol). The reaction mixture was stirred at RT for 1 h and quenched with saturated NaHCO3 solution. The mixture was extracted with DCM (2×) and the combined organic layers were dried, filtered and concentrated under reduced pressure. Purification (FCC, SiO2, 0-80%, EtOAc/hexanes) afforded the title compound as a white solid (73 mg, 64%). [M+H]=381.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102674B2
Source datasetuspto-grants-2015_08
ORD IDord-a99bad42efcb4236a01f49892c1855d7
Source noteuspto-grants-2015_08