HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075711Generated: October 26, 2026
Potassium tert-butoxide → 4-[6-([1,2,4]Triazolo[1,5-a]quinolin-7-ylsulfanyl)-pyridin-2-yl]-tetrahydro-pyran-4-carbonitrile
https://huagongshe.com/reaction/2075711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-(6-Fluoro-pyridin-2-yl)-tetrahydro-pyran-4-carbonitrile | HCID 58257782 | — |
| Reactant | 3-([1,2,4]Triazolo[1,5-a]quinolin-7-ylsulfanyl)-propionic acid 2-ethyl-hexyl ester | HCID 67091107 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[6-([1,2,4]Triazolo[1,5-a]quinolin-7-ylsulfanyl)-pyridin-2-yl]-tetrahydro-pyran-4-carbonitrile | HCID 58257755 | — |
Reaction Steps
8e (201 mg, 0.50 mmol) and 4-(6-Fluoro-pyridin-2-yl)-tetrahydro-pyran-4-carbonitrile (8f, 105 mg, 0.51 mmol) were dissolved in DMF at room temperature and degassed for 10 minutes with N2. Potassium tert-butoxide (67 mg, 0.60 mmol) was added, and the mixture was degassed with N2 for another 10 minutes. The reaction was heated to 90° C. for 12 hours, and then concentrated and purified by silica gel chromatography (25-50% EtOAc in hexanes) to give the desired product, 8g.
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-62db0cd31e9945218522673cca86d3a5 |
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| Source note | uspto-grants-2011_04 |
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