HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638977Generated: November 2, 2026
Triethylamine → 4-Chloro-6-methoxy-1,5-naphthyridine-3-carbonitrile
https://huagongshe.com/reaction/638977
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-6-(methyloxy)-1,5-naphthyridine-3-carboxamide | HCID 68576737 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-6-methoxy-1,5-naphthyridine-3-carbonitrile | HCID 68579101 | 91.1% |
Reaction Steps
To a solution of 4-chloro-6-(methyloxy)-1,5-naphthyridine-3-carboxamide (647 mg, 2.7 mmol) in anhydrous DCM (2 mL) with triethyamine (2 mL) at 0° C. was added trifluororacetic anhydride (1 mL) slowly. The resulting solution was warmed up to 25° C. and stirred for 1 h. The mixture was partitioned between CHCl and H2O. The aqueous layer was extracted several times with CHCl. The organic fractions were combined, concentrated and purified with column chromatography (silica, 0-25% ethyl acetate/hexane) affording the title compound as an off-white solid (540 mg, 91%): LC/MS (ES) m/e 220 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691850B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-6e07b8488a3e49a1857584c7cca8b7f9 |
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| Source note | uspto-grants-2010_04 |
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