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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416222Generated: November 3, 2026

4-Isopropylbenzoic Acid → 2-(4-Isopropylbenzoyl)amino-5-diethylaminoethylthio-1,3,4-thiadiazole

https://huagongshe.com/reaction/1416222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isopropylbenzoic AcidHCID 10820—
ReactantSodium hydrideHCID 24758—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-{[2-(Diethylamino)ethyl]sulfanyl}-1,3,4-thiadiazol-2-amineHCID 314544—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Isopropylbenzoyl)amino-5-diethylaminoethylthio-1,3,4-thiadiazoleHCID 992967994.9%

Reaction Steps

Sodium hydride (0.6 g) and 2-amino-5-diethylaminoethylthio-1,3,4-thiadiazole (2.3 g) were stirred in tetrahydrofuran (30 ml) for 30 minutes while being cooled with ice. 4-Isopropylbenzoic acid (1.6 g) and carbonyldiimidazole (1.8 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 3.5 g of the aimed compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912258
Source datasetuspto-grants-1999_06
ORD IDord-f61cda270da34602b94c2c87dcdfe384
Source noteuspto-grants-1999_06