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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355765Generated: October 30, 2026

o-Phenethylbenzoic acid → HCID 22675471, compound

https://huagongshe.com/reaction/355765

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Phenethylbenzoic acidHCID 78603—
ReactantMethyl 6-aminonicotinateHCID 737487—
ReactantHCID 22675502HCID 22675502—
SolventTolueneHCID 1140—
ProductHCID 22675471HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834468
Source datasetuspto-grants-1998_11
ORD IDord-e672c48d429740d5a9ba4c38eb477398
Source noteuspto-grants-1998_11