HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265633Generated: October 27, 2026
O-Methylhydroxylamine → 2-Amino-6-methoxy-3-nitropyridine
https://huagongshe.com/reaction/265633
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine | HCID 4113 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Methoxy-5-nitropyridine | HCID 79525 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Amino-6-methoxy-3-nitropyridine | HCID 3852428 | 87% |
Reaction Steps
6-Methoxy-3-nitropyridine (154 mg, 1 mmol) and O-methylhydroxylamine (71 mg, 1.5 mmol) were dissolved in DMSO (2 ml), and a resulting solution was added dropwise to a DMSO solution (3 ml) containing potassium tert-butoxide (336 mg, 3 mmol) and zinc (II) chloride (136 mg, 1 mmol) at 25° C. After completion of the addition, the resulting mixture was stirred at 25 ° C. for 9 hours and an aqueous saturated ammonium chloride solution (50 ml) was added, followed by extraction with ethyl acetate (80 ml). A resulting organic layer was dried over anhydrous magnesium sulfate, and then isolated and purified by subjection to silica gel thin layer chromatography [eluent: ethyl acetate/hexane=1/1] to obtain 147 mg of 2-amino-6-methoxy-3-nitropyridine (yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648496 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-e2e437f90535462b87ba39f110724f13 |
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| Source note | uspto-grants-1997_07 |
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