HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497233Generated: October 30, 2026
Methanesulfonic Acid → 6-Chloro-2-(1-ethyl-propyl)-4-phenyl-quinoline-3-carbonitrile
https://huagongshe.com/reaction/1497233
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2-Amino-5-chlorobenzophenone | HCID 12870 | — |
| Reactant | 4-Ethyl-3-oxohexanenitrile | HCID 23505748 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Chloro-2-(1-ethyl-propyl)-4-phenyl-quinoline-3-carbonitrile | HCID 86683053 | 46% |
Reaction Steps
A solution of (2-amino-5-chlorophenyl)(phenyl)methanone (700 mg, 3.02 mmol), 4-ethyl-3-oxo-hexanenitrile (505 mg, 3.63 mmol) and methanesulfonic acid (290 mg, 196 μl, 3.02 mmol) in toluene (40 ml) was stirred for 5 min at room temperature and then heated to reflux using a Dean-Stark-trap to remove water. After 2.5 h the mixture was cooled to room temperature, washed with saturated NaHCO3 solution and water and was evaporated. n-Heptane was added to the remaining residue and the off-white precipitate that formed was filtered off. The precipitate was again dissolved in EtOAc and the solution was washed with saturated NaHCO3 solution and water and was evaporated to yield the title compound (461 mg, 46%) as yellow solid. The filtrate was concentrated and the remaining residue was purified by column chromatography (silica gel, heptane/EtOAc 100:0-0:100) to afford a second batch of the title compound (347 mg, 34%) as yellow solid. MS (ESI): 335.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199938B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-4bbb01a9cef34565ab79bd20ae88f471 |
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| Source note | uspto-grants-2015_12 |
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