HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744735Generated: October 29, 2026
Potassium Carbonate → HCID 10663447, compound
https://huagongshe.com/reaction/744735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-4-(pyridin-3-yl)-1,2,5-thiadiazole | HCID 10488164 | — |
| Reactant | Sodium hydrosulfide hydrate | HCID 16211346 | — |
| Reactant | HCID 21585204 | HCID 21585204 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10663447 | HCID 10663447 | 31% |
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 x 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05559136 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-306e9af4620d4675b5e328aebb6f94ac |
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| Source note | uspto-grants-1996_09 |
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