HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342666Generated: October 27, 2026
3-Aminopyridine → 3-(4-Geranyloxybenzoylamino)pyridine
https://huagongshe.com/reaction/342666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Geranyloxybenzoic acid | HCID 12361500 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Geranyloxybenzoylamino)pyridine | HCID 86753561 | 32.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859032 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-35ddcdabcf344f2ab9564f191d414c50 |
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| Source note | uspto-grants-1999_01 |
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