HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026605Generated: November 3, 2026
Carbon Tetrachloride → HCID 68006085, compound
https://huagongshe.com/reaction/1026605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 68006446 | HCID 68006446 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 68006085 | HCID 68006085 | 41% |
Reaction Steps
A carbon tetrachloride solution (25 ml) of tert-butyl 4-(7-chloro-3,3-dimethyl-2-oxo-3,4-dihydro-1,5-naphthyridin-1(2H)-yl)piperidine-1-carboxylate (Reference Example 10-2) (1.0 g), N-bromosuccinimide (903 mg) and 2,2′-azobisisobutyronitrile (43.2 mg) was heated at reflux for 40 minutes. After the reaction solution was cooled to 0° C., diethylether was added, and filtered through Celite. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to afford tert-butyl 4-(4-bromo-7-chloro-3,3-dimethyl-2-oxo-3,4-dihydro-1,5-naphthyridin-1(2H)-yl)piperidine-1-carboxylate (492 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729095B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-8d2a238e29644c8c8f713dabb7cbd927 |
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| Source note | uspto-grants-2014_05 |
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