HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38089Generated: October 27, 2026
1,2-Dibromoethane → HCID 67424308, compound
https://huagongshe.com/reaction/38089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178509728 | HCID 178509728 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67424308 | HCID 67424308 | 25.9% |
Reaction Steps
3-(5-Mercapto-4-pyridin-4-yl-1H-pyrazol-3-yl)-benzonitrile (4.59 g, 16.1 mmol) was dissolved in dry DMF (200 mL) under nitrogen atmosphere. Solid potassium carbonate (11.1 g, 80.5 mmol, 5 eq) was added followed by 1,2-dibromoethane (1.53 mL, 17.71 mmol, 1.1 eq) and the suspension was stirred at room temperature for 4 hours. The reaction mixture was then concentrated under reduced pressure and diluted with ethyl acetate. It was washed with saturated aqueous NaHCO3 and brine. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude product was treated with methanol and the solid was filtered and discarded. The mother liquor was evaporated to dryness and purified by chromatography on silica gel (eluant DCM/MeOH 97:3) to give 1.27 g of 3-(7-pyridin-4-yl-2,3-dihydro-pyrazolo[5,1-b]thiazol-6-yl)-benzonitrile as a white solid (26% over 2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524707B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-80aec1115d804fa5ade63c9a3579766b |
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| Source note | uspto-grants-2013_09 |
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