HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922812Generated: November 1, 2026
Ammonia methanol → 7-[2-(6-Cyanopyridin-3-yl)ethyl]-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxamide
https://huagongshe.com/reaction/922812
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | Methyl 7-[2-(6-cyanopyridin-3-yl)ethyl]-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxylate | HCID 89543747 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-[2-(6-Cyanopyridin-3-yl)ethyl]-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxamide | HCID 89543782 | 67.9% |
Reaction Steps
A stirred solution of methyl 7-[2-(6-cyanopyridin-3-yl)ethyl]-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxylate (160 mg, 0.362 mmol) and MeOH (1450 μl) was treated with 5 ml 7N NH3/MeOH and then heated to 60° C. in a sealed tube for 30 minutes. The reaction was allowed to cool to ambient temperature and then was concentrated. The solid was trituated with EtOH, collected, washed with 5 ml Et2O and then dried in vacuo to afford 7-[2-(6-cyanopyridin-3-yl)ethyl]-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carboxamide (105 mg, 0.246 mmol, 67.9% yield) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278960B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0d93acef2ed541709a4fe39b51bf996c |
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| Source note | uspto-grants-2016_03 |
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