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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant4-PiperidoneHCID 33721—
ReactantBenzamide, 5-(acetylamino)-2-hydroxy-HCID 10330248—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductSpiro[2H-1,3-benzoxazine-2,4'-piperidin]-4(3H)-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110570B2
Source datasetuspto-grants-2012_02
ORD IDord-764a21ddb1184ccebf879e23a3e47f8b
Source noteuspto-grants-2012_02