HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422938Generated: October 30, 2026
Hydrogen Peroxide → 3-Benzyloxy-6-methoxy-[1,5]naphthyridine-4-carboxylic acid amide
https://huagongshe.com/reaction/1422938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Benzyloxy-6-methoxy-[1,5]naphthyridine-4-carbonitrile | HCID 67257004 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Benzyloxy-6-methoxy-[1,5]naphthyridine-4-carboxylic acid amide | HCID 67253981 | 75% |
Reaction Steps
30% Hydrogen peroxide (17.2 mmol, 5.0 eq) is added dropwise at room temperature to a stirred suspension of 3-benzyloxy-6-methoxy-[1,5]naphthyridine-4-carbonitrile (1.0 g, 3.43 mmol, 1.0 eq) and sodium hydroxide (69 mg, 0.17 mmol, 0.05 eq) in methanol (100 mL). After 1 hour stirring at 70° C., a catalytic amount of manganese dioxide is added to the reaction mixture that is concentrated to give a crude that is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 1:1, v/v) to afford 3-benzyloxy-6-methoxy-[1,5]naphthyridine-4-carboxylic acid amide as a white solid (800 mg, 75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08927541B2 |
|---|
| Source dataset | uspto-grants-2015_01 |
|---|
| ORD ID | ord-351f8f2aa16745a0bef44f96a1d9293d |
|---|
| Source note | uspto-grants-2015_01 |
|---|