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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376627Generated: November 1, 2026

Trifluoromethanesulfonic acid → 6-Trifluromethanesulfonyl-8-(3 cyanophenyl)-1,7-naphthyridine

https://huagongshe.com/reaction/2376627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant3-(6-Amino-1,7-naphthyridin-8-yl)benzonitrileHCID 10705571—
ReactantSodium NitriteHCID 23668193—
SolventDimethylformamideHCID 6228—
Product6-Trifluromethanesulfonyl-8-(3 cyanophenyl)-1,7-naphthyridineHCID 17896283—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-amino-8-(3-cyanophenyl)-1,7-naphthyridine (4.058 g) in dimethyl-formamide (DMF) (22 ml) under argon at 0° C. is added trifluoromethanesulfonic acid (11 ml). The mixture is stirred at 0° C. for 10 minutes and then sodium nitrite (2.26 g) is added slowly. The cooling bath is then removed and the mixture stirred at room temperature for 3 hours. The resulting mixture is diluted with ethyl acetate and washed with water, 2M NaOH and water again. The organic layer is dried over sodium sulfate, then concentrated in vacuo and purified by column chromatography, eluting with 10:0.5 toluene:acetone to yield the title compound. M.p. 102-104° C. MS (m/e)=380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468370B2
Source datasetuspto-grants-2008_12
ORD IDord-83f32037ac3943768f0eca4b17857ce6
Source noteuspto-grants-2008_12