HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075720Generated: October 31, 2026
Glycol monoethyl ether → 1,1,1-Trifluoro-2-[2-(1-phenyl-[1,2,4]triazolo[4,3-a]quinolin-7-ylsulfanyl)-thiazol-5-yl]-butan-2-ol
https://huagongshe.com/reaction/2075720
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycol monoethyl ether | HCID 8076 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Iodo-1-phenyl-[1,2,4]triazolo[4,3-a]quinoline | HCID 58257758 | — |
| Reactant | HCID 178472193 | HCID 178472193 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,1,1-Trifluoro-2-[2-(1-phenyl-[1,2,4]triazolo[4,3-a]quinolin-7-ylsulfanyl)-thiazol-5-yl]-butan-2-ol | HCID 67090867 | — |
Reaction Steps
7-Iodo-1-phenyl-[1,2,4]triazolo[4,3-a]quinoline (10c, 140 mg, 0.38 mmol), copper iodide (14 mg, 0.08 mmol), and potassium carbonate (105 mg, 0.76 mmol) were suspended in iPrOH (1 mL). 10b (92 mg, 0.38 mmol) in iPrOH (1 mL) was added, followed by ethyl glycol (0.04 mL, 0.76 mmol), and the reaction was heated to 90° C. overnight. The reaction was diluted with EtOAc and water, and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel chromatography (5% MeOH in CH2Cl2), and the isolated product was precipitated from CH2Cl2 to give the desired product, 10d.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919621B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-b99293a7aa1346f4922e1fa8c3d16d6e |
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| Source note | uspto-grants-2011_04 |
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