反应 #1726709

反应方程式

4-piperidone

5-acetamido-2-hydroxybenzamide

morpholine

→

Compound 9

spiro[2H-1,3-benzoxazin-2,4′-piperidin]-4-(3H)-one

溶剂

ethyl acetate

methanol

反应条件

后处理

1. 1
   温度is refluxed for 48 hr
2. 2
   洗涤washed with water, brine
3. 3
   干燥dried over Na2SO4
4. 4
   其他After solvent removal by rotoevaporation
5. 5
   其他the crude product is purified by preparative TLC

实验过程

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)+.

来源