HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120071Generated: October 31, 2026
Hydrochloric Acid → Ethyl 5-aminopyridine-2-carboxylate
https://huagongshe.com/reaction/2120071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Aminopyridine-2-carboxylic acid | HCID 4179726 | — |
| Product | Ethyl 5-aminopyridine-2-carboxylate | HCID 13816714 | — |
Reaction Steps
A stirred suspension of 3-amino-pyridine-6-carboxylic acid (25 g) in ethanol (300 mL) at 0° C. was saturated with gaseous hydrogen chloride. The mixture was allowed to warm to 23° C. and heated to reflux for 2 hours. A clear solution was obtained. After cooling to 23° C., the mixture was concentrated in vacuo, neutralized with aqueous NaHCO3 and extracted with ethyl acetate. The organic phase was washed with water, dried over MgSO4, and concentrated in vacuo to give ethyl 3-amino-pyridine-6-carboxylate as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689754B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-2d07cdb8725146c799a144402ccdec56 |
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| Source note | uspto-grants-2004_02 |
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