HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832042Generated: October 31, 2026
N-Bromosuccinamide → HCID 22050819, compound
https://huagongshe.com/reaction/1832042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Reactant | HCID 22051183 | HCID 22051183 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22050819 | HCID 22050819 | — |
Reaction Steps
In a 50 ml one neck round bottom flask 4-[(2,4-difluorobenzyl)oxy]-1-(2,6-difluorophenyl)-6-oxo-1,6-dihydropyridine-2-carbaldehyde (0.36 g, 0.95 mmol) was dissolved in acetonitrile (5 mL). The reaction mixture was cooled to 0° C. in ice bath and charged with N-bromosuccinamide (0.17 g, 0.95 mmol). The mixture was allowed to stir at 0° C. for 2 hours under nitrogen atmosphere After 2 hours, the solvent was evaporated under vacuum. 1H NMR (400 MHz, DMSO-d6) δ 9.53 (s, 1H), 7.73-7.67 (m, 2H), 7.62-7.54 (m, 1H), 7.35 (dt, J=10.40, 2.56 Hz, 1H), 7.27 (t, J=8.35 Hz, 2H), 7.19 (dt, J=8.60, 2.44 Hz, 1H), 5.72 (s, 1H), 5.50 (s, 2H); ES-MS m/z 455.9836 (M+H calcd for C19H11BrF4NO3, requires 455.9859).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067540B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-0b81705f3bd640868a09f3867b1f1f7e |
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| Source note | uspto-grants-2006_06 |
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