HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803767Generated: November 1, 2026
2,3-Dihydro-1-methyl-4(1H)-quinolinone → HCID 87105755, compound
https://huagongshe.com/reaction/1803767
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Dihydro-1-methyl-4(1H)-quinolinone | HCID 420419 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 87105755 | HCID 87105755 | — |
Reaction Steps
Methoxylamine hydrochloride (0.88 g, 10.6 mmol) was added to a solution of Example 17A (1.55 g, 9.6 mmol) in pyridine (20 mL) and the mixture stirred overnight at ambient temperature. The mixture was concentrated under reduced pressure and ethyl acetate (200 mL) was added. The organic layer was washed twice with water (200 mL) and brine, dried over sodium sulfate, filtered, and concentrate under reduced pressure. The residue was chromatographed on silica gel eluting with 0-20% ethyl acetate in hexane to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 2.76 (t, J=6.61 Hz, 2H), 2.83 (s, 3H), 3.11 (t, J=6.61 Hz, 2H), 3.87 (s, 3H), 6.69 (t, J=7.46 Hz, 1H), 6.75 (d, J=8.48 Hz, 1H), 7.22 (td, J=7.80, 1.70 Hz, 1H), 7.73 (dd, J=7.80, 1.70 Hz, 1H). MS (DCI) m/z 191.07 (M+H)1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08350083B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-e9ce108ee4794726bc80d492d537cb21 |
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| Source note | uspto-grants-2013_01 |
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