HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601673Generated: October 29, 2026
Sodium Acetate → 4-(thiazolo[5,4-b]pyridine-2-yl)-1-(2-chlorophenyl)-5-methyl-1H-[1,2,3]triazole
https://huagongshe.com/reaction/601673
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Thiazolo(5,4-b)pyridine | HCID 19831912 | — |
| Reactant | 1-(2-Chlorophenyl)-4-iodo-5-methyl-[1,2,3]-triazole | HCID 23158267 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(thiazolo[5,4-b]pyridine-2-yl)-1-(2-chlorophenyl)-5-methyl-1H-[1,2,3]triazole | HCID 23158160 | 8.5% |
Reaction Steps
Under nitrogen atmosphere, 344 mg of 1-(2-chlorophenyl)-4-iodo-5-methyl-[1,2,3]-triazole and 276 mg of thiazolo(5,4-b)pyridine (B. Stanovnik, Synthesis, 1974, 120) were dissolved in 3 ml of DMF. Then, 100 mg of sodium acetate and 103 mg of Herrman catalyst were added, and the mixture was stirred at 140° C. for 8 hours. After diluting the reaction solution with water, the resultant was extracted with chloroform. Organic layer was washed with saturated saline solution, and dried with anhydrous sodium sulfate. The residues obtained by distilling out the solvents were separated and purified by thin-layer silicagel column chromatography (ethyl acete/hexane=1/1) to obtain 30 mg of the above compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902369B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-5b3301b88e2c4c008ac9c0ca8bedb795 |
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| Source note | uspto-grants-2011_03 |
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