Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 4-Geranyloxybenzoic acid | HCID 12361500 | — |
| Reactant | HCID 17137380 | HCID 17137380 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9806018 | HCID 9806018 | 78.8% |
Reaction Steps
Sodium hydride (0.4 g) and 2-amino-5-piperidinoethylthio-1,3,4-thiadiazole (1.5 g) were stirred in tetrahydrofuran (30 ml) for 30 minutes while being cooled with ice. 4-Geranyloxybenzoic acid (1.6 g) and carbonyldiimidazole (1.1 g) were stirred in tetrahydrofuran (30 ml) for 30 minutes at room temperature and the mixture was added to the former reaction mixture. The mixture was stirred for 4 hours at room temperature, and then 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/ethanol, thereby yielding 2.3 g of the aimed compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05912258 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-434f1fd2b1fb4747af4e08ae7626f136 |
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| Source note | uspto-grants-1999_06 |
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