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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898967Generated: October 30, 2026

Potassium Carbonate → HCID 10663447, compound

https://huagongshe.com/reaction/1898967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-4-(pyridin-3-yl)-1,2,5-thiadiazoleHCID 10488164—
ReactantSodium hydrosulfide hydrateHCID 16211346—
ReactantHCID 21585204HCID 21585204—
SolventDimethylformamideHCID 6228—
ProductHCID 10663447HCID 1066344731%

Reaction Steps

A solution of 3-(3-chloro-1,2,5-thiadiazol-4-yl)pyridine (2.0 g, 10.1 mmol) in DMF (10 ml) was cooled to 5° C. whereupon potassium carbonate (2.8 g, 20.2 mmol) and sodium hydrosulfide monohydrate (1.5 g, 20.2 mmol) were added to the reaction. Stirred for 1 h then potassium carbonate (1.4 g, 10.1 mmol) and a solution of 3-(2-thienyl)-1-chloro-propane (1.8 g, 11.2 mmol) in DMF (5 ml) were added to the reaction and stirred for 1 h at room temperature. The reaction was quenched with water then extracted with methylene chloride (3×75 ml). The organic phase was dried over NaCl/Na2SO4 then evaporated. The residue was purified by flash chromatography eluting with 1:1 ethyl acetate/hexanes to yield 1.0 g of 3-(3-(3-(2-thienyl)-1-propylthio)-1,2,5-thiadiazol-4-yl) pyridine. Quaternization and reduction was done as described in example 9. (Compound 66). M.p. 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571826
Source datasetuspto-grants-1996_11
ORD IDord-3f2f93c8247d417c938767d011663367
Source noteuspto-grants-1996_11