HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105505Generated: November 3, 2026
m-Chloroperbenzoic acid → HCID 67505829, compound
https://huagongshe.com/reaction/2105505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67505846 | HCID 67505846 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67505829 | HCID 67505829 | 99.9% |
Reaction Steps
A solution of 2-butyl-1-isopropoxy-1H-imidazo[4,5-c][1,5]naphthyridine (0.40 g, 1.4 mmol) in dichloromethane (25 mL) was cooled to approximately 0° C., and 3-chloroperoxybenzoic acid (0.42 g of approximately 77% pure material, 1.9 mmol) was added. The reaction was stirred for ten minutes at 0° C., stirred for 1.5 hours at room temperature, and then stirred with saturated aqueous sodium bicarbonate (25 mL) for 15 minutes. The organic layer was separated and dried over potassium carbonate, filtered, and concentrated under reduced pressure to provide 0.42 g of 2-butyl-1-isopropoxy-5-oxido-1H-imidazo[4,5-c][1,5]naphthyridine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579359B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-40f1b61f4dc943f4ae6fb9be3948a82f |
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| Source note | uspto-grants-2009_08 |
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