HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279424Generated: October 29, 2026
N-bromobutanimide → HCID 178487833, compound
https://huagongshe.com/reaction/2279424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 178487891 | HCID 178487891 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178487833 | HCID 178487833 | 97% |
Reaction Steps
N-Bromosuccinimide (263 mg, 1.48 mmol, 1.3 eq) is added at 15° C. to a stirred solution of 6-methoxy-[1,5]naphthyridin-4-ol (200 mg, 1.14 mmol, 1.0 eq) in acetic acid (3 mL). After 30 minutes stirring at 15° C., the reaction mixture is allowed to come at room temperature and the resulting cake is filtered, washed with acetic acid and dried to afford 3-bromo-6-methoxy-[1,5]naphthyridin-4-ol as an off-white solid (280 mg, 97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133219B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-485e4ec02d84414d902e065ee15a946b |
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| Source note | uspto-grants-2015_09 |
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