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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | 3-(6-Amino-1,7-naphthyridin-8-yl)benzonitrile | HCID 10705571 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Trifluromethanesulfonyl-8-(3 cyanophenyl)-1,7-naphthyridine | HCID 17896283 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468370B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-83f32037ac3943768f0eca4b17857ce6 |
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| Source note | uspto-grants-2008_12 |
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