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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651444Generated: October 27, 2026

Hydrochloric Acid → 3-(3-Pentylthio-1,2,5-thiadiazol-4-yl)-1-azabicyclo[2.2.2]octane fumarate

https://huagongshe.com/reaction/651444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-BromopentaneHCID 8057—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Chloro-1,2,5-thiadiazol-4-yl)-1-azabicyclo[2.2.2]octane oxalateHCID 21708545—
ReactantSodium hydrogen sulfide hydrateHCID 53442613—
SolventDimethylformamideHCID 6228—
Product3-(3-Pentylthio-1,2,5-thiadiazol-4-yl)-1-azabicyclo[2.2.2]octane fumarateHCID 21708571—

Reaction Steps

A solution of 3-(3-chloro-1,2,5-thiadiazol-4-yl)-1-azabicyclo[2.2.2]octane oxalate (500 mg, 1.56 mmol), sodiumhydrogen sulfide, monohydrate (463 mg, 6.25 mmol) and potassium carbonate (1.38 g, 10 mmol) in DMF (20 ml) was stirred at room temperature for 1 h. 1-Pentylbromide (755 mg, 5 mmol) was added, and the reaction mixture was stirred at room temperature for 18 h. 1 N HCl was added, and the mixture extracted with ether once. 50% NaOH was added to the aqueous phase and extracted with ether. The ether phase was dried and evaporated. Crystallization of the residue with fumaric acid from isopropanol/ether gave the title compound in 380 mg yield. (Compound 12). M.p. 138-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281233B1
Source datasetuspto-grants-2001_08
ORD IDord-e62f7e8297644ac29dec463a37229185
Source noteuspto-grants-2001_08