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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342666Generated: October 27, 2026

3-Aminopyridine → 3-(4-Geranyloxybenzoylamino)pyridine

https://huagongshe.com/reaction/342666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
ReactantSodium hydrideHCID 24758—
Reactant4-Geranyloxybenzoic acidHCID 12361500—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Geranyloxybenzoylamino)pyridineHCID 8675356132.4%

Reaction Steps

Sodium hydride(0.74 g) and 3-aminopyridine(0.87 g) were stirred in tetrahydrofuran(30 ml) for 1 hour while being cooled with ice. 4-geranyloxybenzoic acid(2.54 g) and N,N'-carbonyldiimidazole(1.65 g) was stirred in tetrahydrofuran(10 ml) for 30 minutes at room temperature and the mixture was added to the former reaction mixture. After being stirred for 20 minutes at room temperature, the reaction mixture was concentrated under a vacuum. The residue, with water added thereto, was extracted with ethyl acetate. The extract was dried over sodium sulfate anhydride and then concentrated under a vacuum. The residue was purified by silica gel column chromatography (chloroform:methanol=20:1). The resulting solid was recrystallized from n-hexane/ethyl acetate, thereby yielding 1.05 g of the aimed compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859032
Source datasetuspto-grants-1999_01
ORD IDord-35ddcdabcf344f2ab9564f191d414c50
Source noteuspto-grants-1999_01