HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639527Generated: October 26, 2026
Morpholine → Spiro[2H-1,3-benzoxazine-2,4'-piperidin]-4(3H)-one
https://huagongshe.com/reaction/1639527
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 4-Piperidone | HCID 33721 | — |
| Reactant | Benzamide, 5-(acetylamino)-2-hydroxy- | HCID 10330248 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Spiro[2H-1,3-benzoxazine-2,4'-piperidin]-4(3H)-one | HCID 379969 | — |
Reaction Steps
A mixture of 24 mg (0.077 mmol) of N-[4,8-dimethoxyquinoline-2-yl)carbonyl]-4-piperidone, 15 mg (0.077 mmol) of 5-acetamido-2-hydroxybenzamide, and 0.020 mL of morpholine in 3 mL of methanol is refluxed for 48 hr. The reaction mixture is diluted with ethyl acetate, and washed with water, brine, and dried over Na2SO4. After solvent removal by rotoevaporation, the crude product is purified by preparative TLC to give 11 mg (0.022 mmol, 30% yield) of 6-acetamido-1′-[4,8-dimethoxyquinoline-2-yl)carbonyl]spiro[2H-1,3-benzoxazin-2,4′-piperidin]-4-(3H)-one (Compound 9): 1H NMR (DMSO-d6): δ 2.02 (s, 3H), 3.95 (s, 3H), 4.06 (s, 3H), 7.03 (d, 1H), 8.19 (s, 1H), 7.24 (d of d, 1H), 7.52 (d of d, 1H), 7.67 (m, 2H), 8.02 (d, 1H), 8.82, (s, 1H) and 9.98 ppm (s, 1H). MS m/z: 491.1 (M+H)+, 513.2 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110570B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-764a21ddb1184ccebf879e23a3e47f8b |
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| Source note | uspto-grants-2012_02 |
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