HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416229Generated: November 2, 2026
Sodium hydride → 2-(4-Geranyloxybenzoyl)amino-5-diethylaminoethylthio-1,3,4-thiadiazole
https://huagongshe.com/reaction/1416229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 5-{[2-(Diethylamino)ethyl]sulfanyl}-1,3,4-thiadiazol-2-amine | HCID 314544 | — |
| Reactant | 4-Geranyloxybenzoic acid | HCID 12361500 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Geranyloxybenzoyl)amino-5-diethylaminoethylthio-1,3,4-thiadiazole | HCID 9957157 | 87.7% |
Reaction Steps
Sodium hydride (0.4 g) and 2-amino-5-diethylaminoethylthio-1,3,4-thiadiazole (1.4 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 2.5 g of the aimed compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05912258 |
|---|
| Source dataset | uspto-grants-1999_06 |
|---|
| ORD ID | ord-20e6511a575243a7b391ee48dee0723d |
|---|
| Source note | uspto-grants-1999_06 |
|---|