HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15122Generated: October 25, 2026
Water → 8-Bromo-7-chloro-2-methoxy-1,5-naphthyridine
https://huagongshe.com/reaction/15122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | 3-Chloro-6-methoxy-[1,5]naphthyridin-4-ol | HCID 57418810 | — |
| Reactant | HCID 178487877 | HCID 178487877 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-Bromo-7-chloro-2-methoxy-1,5-naphthyridine | HCID 51358223 | 91% |
Reaction Steps
To a solution of 3-chloro-6-(methyloxy)-1,5-naphthyridin-4(1H)-one (3-chloro-6-(methoxy)-1,5-naphthyridin-4-ol, for a synthesis see WO2004058144, Example 1(a)) (43 g, 204.8 mmol) in N,N-dimethylformamide (500 ml) at 0° C. was added phosphorous tribromide dropwise (23.3 ml, 245.8 mmol). The reaction mixture was then stirred at 10° C. for 0.5 hour and then at 25° C. for 1 hour. The mixture was then poured onto 1600 ml of water and basified to pH 7 with potassium carbonate. The solid formed was filtered off, washed with water and dried in vacuo to afford the desired compound (51 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732460B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-e71f60717c35491292adc3deb5bf6d24 |
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| Source note | uspto-grants-2010_06 |
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