HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803763Generated: November 1, 2026
O-Methylhydroxylamine hydrochloride → HCID 87105706, compound
https://huagongshe.com/reaction/1803763
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | 1-benzyl-1,2,3,4-tetrahydroquinolin-4-one | HCID 20142718 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 87105706 | HCID 87105706 | — |
Reaction Steps
Methoxyl amine hydrochloride (0.74 g, 8.9 mmol) was added to a solution of Example 15C (1.92 g, 8.1 mmol) in pyridine (20 mL) and stirred overnight at ambient temperature. The mixture was concentrate under reduced pressure, ethyl acetate (200 mL) was added, and 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, CDCl3) δ ppm 2.88 (t, J=6.44 Hz, 2H), 3.29 (t, J=6.44 Hz, 2H), 3.97 (s, 3H), 4.47 (s, 2H), 6.65 (d, J=8.14 Hz, 1H), 6.70 (t, J=7.46 Hz, 1H), 7.13 (td, J=7.80, 1.70 Hz, 1H), 7.31 (m, 5H), 7.92 (dd, J=7.80, 1.70 Hz, 1H). MS (DCI) m/z 267.11 (M+H)+.
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-a8407e98b1734863ba0b961c11e536ed |
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| Source note | uspto-grants-2013_01 |
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