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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-{[2-(Diethylamino)ethyl]sulfanyl}-1,3,4-thiadiazol-2-amineHCID 314544—
Reactant4-Geranyloxybenzoic acidHCID 12361500—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Geranyloxybenzoyl)amino-5-diethylaminoethylthio-1,3,4-thiadiazoleHCID 995715787.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912258
Source datasetuspto-grants-1999_06
ORD IDord-20e6511a575243a7b391ee48dee0723d
Source noteuspto-grants-1999_06