HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168384Generated: November 1, 2026
m-Chloroperbenzoic acid → HCID 22992260, compound
https://huagongshe.com/reaction/1168384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | HCID 22172705 | HCID 22172705 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22992260 | HCID 22992260 | — |
Reaction Steps
3-Chloroperbenzoic acid (3.7 g, 13.4 mmol) was added in 3 portions to a solution of 2-ethoxymethyl-1-phenylmethyl-1H-imidazo[4,5-c][1,5]naphthyridine (3.9 g, 12.2 mmol) in chloroform (100 mL) in a flask covered with aluminum foil. The reaction mixture was stirred at ambient temperature overnight; and then it was washed twice with dilute aqueous sodium bicarbonate and once with brine. The chloroform layer was divided into two portions. One portion was used in the example below. The second portion was concentrated under vacuum. The residue was recrystallized from isopropyl alcohol to provide 2-ethoxymethyl-1-phenylmethyl-1H-imidazo[4,5-c][1,5]naphthyridine-5-oxide as a solid, m.p. 187.5-189° C. Analysis: Calculated for C19H18N4O2+¼ H2O: %C, 67.52; %H, 5.49; %N, 16.58; Found: %C, 67.56; %H, 5.36; %N, 16.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06624172B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-9a1be3ed713c4bfe86907574919bcbd3 |
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| Source note | uspto-grants-2003_09 |
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