HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Phenethylbenzoic acid → HCID 22675471, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Phenethylbenzoic acid | HCID 78603 | — |
| Reactant | Methyl 6-aminonicotinate | HCID 737487 | — |
| Reactant | HCID 22675502 | HCID 22675502 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22675471 | HCID 22675471 | — |
Reaction Steps
Methyl 2-[N-(2-(phenethyl)benzyl)amino]pyridine-5-carboxylate was prepared from methyl 2-amino-5-pyridinecarboxylate and 2-phenethylbenzoic acid by a procedure similar to that described in Example 4 paragraph (G), except that the imine intermediate, methyl 2-[N-(2-(phenethyl)benzylidene)amino]-5-pyridinecarboxylate, was formed by heating methyl 2-amino-5-pyridinecarboxylate and 2-phenethylbenzoic acid in a Dean & Starke apparatus in toluene for 18 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834468 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-e672c48d429740d5a9ba4c38eb477398 |
| Source note | uspto-grants-1998_11 |