HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945428Generated: November 2, 2026
Methyl 2-aminopyridine-4-carboxylate → HCID 24811989, compound
https://huagongshe.com/reaction/1945428
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-aminopyridine-4-carboxylate | HCID 236984 | — |
| Reactant | PMID26882240-Compound-8 | HCID 625381 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 24811989 | HCID 24811989 | 75.5% |
Reaction Steps
To a solution of appropriate (4-adamantan-1-yl-phenoxy)-acetic acid (150 mg, 0.523 mmol), 2-amino isonicotinic acid methyl ester (159.3 mg, 1.04 mmol) and DMAP (127.9 mg, 1.04 mmol) in DMF (6 ml) was added PyBOP (545 mg, 1.04 mmol) at room temperature and the resulting mixture was stirred until reaction completion as indicated by TLC. Reaction mixture was poured onto ice cold water, diluted with ethyl acetate, separated organic layer and sequentially washed with aqueous sodium bicarbonate, brine and water, and dried over anhydrous MgSO4. The solvent was filtered and evaporated under reduced pressure to afford a crude solid, which was purified by flash chromatography on silica gel (EtOAc:hexanes=1:9 to 1:1) to afford of 2-[2-(4-adamantan-1-yl-phenoxy)acetylamino]-isonicotinic acid methyl ester as a colorless solid (0.166 g, 75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394799B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d902aca7166240b39eb5f6d4dc86bfaa |
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| Source note | uspto-grants-2013_03 |
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