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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991698Generated: October 27, 2026

Ethylene Glycol → tert-Butyl 4-[4-(2-hydroxyethoxy)-1,2,5-thiadiazol-3-yl]-1-piperazinecarboxylate

https://huagongshe.com/reaction/991698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTert-butyl 4-(4-chloro-1,2,5-thiadiazol-3-yl)piperazine-1-carboxylateHCID 15524001—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-[4-(2-hydroxyethoxy)-1,2,5-thiadiazol-3-yl]-1-piperazinecarboxylateHCID 2203639379.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

K-t-BuO (1.24 g, 11 mmol) was added to a mixture of the product obtained in Step 1 (1.98 g, 6.5 mmol) and ethylene glycol (2.54 ml, 45.5 mmol) in pyridine (15 ml). The reaction mixture was stirred at 100° C. for 6 h and at room temperature overnight. The solution was then poured into ice-water and diluted with EtOAc. The organic phase was dried (MgSO4) and the solvent removed under reduced pressure. The residue was purified by chromatography on silica gel eluting hexane/EtOAc (1:1) to give 1.71 g (65%) of title product as an orange oil. MS m/z 331 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465467B1
Source datasetuspto-grants-2002_10
ORD IDord-6b104a18cb7f42f6ac85c0c2a990caea
Source noteuspto-grants-2002_10