HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668556Generated: October 31, 2026
Acetic Acid → 3-{5-[(3-Chloropropyl)thio]-4-methyl-4H-1,2,4-triazol-3-yl}pyridine
https://huagongshe.com/reaction/1668556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | 4-methyl-5-(pyridin-3-yl)-4H-1,2,4-triazole-3-thiol | HCID 757582 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-{5-[(3-Chloropropyl)thio]-4-methyl-4H-1,2,4-triazol-3-yl}pyridine | HCID 53417310 | — |
Reaction Steps
To 4-methyl-5-(3-pyridinyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione (0.4 g, preparation reported in WO 02/40471) in ethanol (6 ml) sodium ethanolate (0.85 ml) was carefully added with stirring followed by 1-bromo-3-chloropropane (0.31 ml). The mixture was heated at 90° C. for 1 h. Acetic acid was added at room temperature until pH=4. After elimination of the solvent under reduced pressure the residue was partitioned between aqueous NaHCO3 (saturated) and DCM. The organic layer was collected and the aqueous phase extracted twice with DCM. The combined DCM layers were concentrated and submitted to column chromatography (EtOAc—acetone gradient) to provide the title compound as white solid (0.360 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989444B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-29b55d647dbc4c9883f5c8428c22482e |
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| Source note | uspto-grants-2011_08 |
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