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HRID 1639527생성일: 2026년 10월 27일

Morpholine → Spiro[2H-1,3-benzoxazine-2,4'-piperidin]-4(3H)-one

https://huagongshe.com/reaction/1639527

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물4-PiperidoneHCID 33721—
반응물Benzamide, 5-(acetylamino)-2-hydroxy-HCID 10330248—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물Spiro[2H-1,3-benzoxazine-2,4'-piperidin]-4(3H)-oneHCID 379969—

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08110570B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-764a21ddb1184ccebf879e23a3e47f8b
출처 메모uspto-grants-2012_02