HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-aminopyridine-4-carboxylate → HCID 20275365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-aminopyridine-4-carboxylate | HCID 236984 | — |
| Reactant | Methyl 2-aminopyridine-3-carboxylate | HCID 351633 | — |
| Reactant | 2-[(Acetylthio)methyl]-3-phenylpropionic Acid | HCID 9991796 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20275365 | HCID 20275365 | — |
Reaction Steps
Following the procedure of Example 1, but substituting an equivalent amount of methyl 2-amino-isonicotinate and 2-acetylthiomethyl-3-phenyl-propionic acid respectively for methyl 2-amino-nicotinate and 2-acetylthiomethyl-3-phenyl-propionic acid, using pyridine as reaction solvent, maintaining the reaction mixture at 50°-60° C. for five hours and purifying by chromatography on silica gel column (eluent, petroleum ether/ether 7:3), methyl 2-(2-acetylthiomethyl-3-phenyl-propionamido)-isonicotinate is obtained as an oil which is transformed into the corresponding hydrochloride with an alcoholic solution of hydrogen chloride; m.p. 137°-139° C., from acetone/ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528296 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-66ffdc42ad014c4a885ea754e250889e |
| Source note | uspto-grants-1985_07 |