HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013729Generated: October 30, 2026
2,3-Dimethoxy-5-nitropyridine → 5,6-Dimethoxypyridin-3-amine
https://huagongshe.com/reaction/1013729
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dimethoxy-5-nitropyridine | HCID 3848744 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5,6-Dimethoxypyridin-3-amine | HCID 12758214 | — |
Reaction Steps
A stainless steel bomb was charged with 2,3-dimethoxy-5-nitropyridine (430 mg, 2335 μmol), 10% Pd/C (124 mg, 1168 μmol) and 4.7 mL EtOAc. The vessel was sealed and was purged with hydrogen once, before filling with hydrogen at a pressure of 2 attn. The reaction mixture was heated at 50° C. for 3 h. Upon cooling, the mixture was filtered through a pad of Celite, rinsing with EtOAc. The filtrate was concentrated and passed through a silica plug using 5% MeOH/DCM. The filtrate was concentrated to provide 5,6-dimethoxypyridin-3-amine as a peach colored oil that crystallized upon standing. GC/MS confirmed the correct mass to be [M+H]=155.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981891B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-799a467a0bac4a9580b4b9434332a1ab |
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| Source note | uspto-grants-2011_07 |
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