HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217899Generated: October 28, 2026
Benzoyl Peroxide → HCID 69023349, compound
https://huagongshe.com/reaction/217899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 69026638 | HCID 69026638 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69023349 | HCID 69023349 | 59.2% |
Reaction Steps
To a solution of 0.080 g (0.24 mmol) of (4-oxo-2-pyrimidin-4-yl -4,6,7,8,9,10-hexahydro-pyrimido[1,2-a]azepin-10-yl)-carbamic acid ethyl ester in dimethylformamide (4 mL) were added 0.21 g (1.21 mmol) of N-bromosuccinimide and 0.03 g (0.12 mmol) of benzoyl peroxide. The solution was stirred at room temperature for 10 min and at 50° C. for 20 min. The reaction was quenched by adding a saturated solution of ammonium chloride. The product was extracted with dichloromethane, the organic phase was washed with a saturated solution of sodium chloride, dried over sodium sulfate, filtered and the solvent was evaporated. The residue was chromatographed on silica gel eluting with a mixture of dichloromethane/methanol in the proportions 95/5 to afford 58 mg of a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198287B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-8b9ae9c1b674455098d2a6e2ea635048 |
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| Source note | uspto-grants-2012_06 |
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