Synlett 2018; 29(05): 617-620
DOI: 10.1055/s-0036-1591522
letter
© Georg Thieme Verlag Stuttgart · New York

Metal-Free Cascade Methylation/Cyclization of N-Alkyl-N-methacryloylbenzamides with Dicumyl Peroxide

Yan-Ning Niu*
a   Department of Teaching and Research, Nanjing Forestry University, Huaian, Jiangsu, 223003, P. R. of China.   eMail: zjsnyn@163.com
,
Xiao-Feng Xia*
b   Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, Jiangsu, 214122, P. R. of China.   eMail: xiaxf@jiangnan.edu.cn
,
Yuan Yuan
a   Department of Teaching and Research, Nanjing Forestry University, Huaian, Jiangsu, 223003, P. R. of China.   eMail: zjsnyn@163.com
› Institutsangaben
We thank the National Science Foundation of China NSF 21402066, the Natural Science Foundation of Jiangsu Province (BK20140139), the science and technology plan project of Huaian (HAGZ201614), and MOE&SAFEA for the 111 project (B13025) for financial support.
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Publikationsverlauf

Received: 14. Oktober 2017

Accepted after revision: 18. November 2017

Publikationsdatum:
20. Dezember 2017 (online)


Abstract

A metal-free radical cascade methylation/cyclization of a wide range of N-alkyl-N-methacryloylbenzamides by using dicumyl peroxide as the methylating reagent provides a convenient access to a series of methylated isoquinoline-1,3-diones in moderate yields.

Supporting Information

 
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  • 9 4-Ethyl-2,4-dimethylisoquinoline-1,3(2H,4H)-dione (3a); Typical Procedure DCP (0.6 mmol) was added to a stirred solution of N-methacryloyl-N-methylbenzamide (1a; 0.2 mmol) in PhCl (1.0 mL) in a test tube. The tube was sealed, and the mixture was stirred at 120 °C for 17 h. H2O (5 mL) was added to quench the reaction, and the mixture was extracted with EtOAc (3 × 10 mL). The organic layers were combined, washed with sat. aq NaCl (2 × 10 mL), dried (Na2SO4), and concentrated. The residue was purified by column chromatography [silica gel, hexanes–EtOAc (8:1)] to give a colorless oil; yield; 26 mg (60%).IR (KBr): 3066, 2966, 2934, 2876, 1714, 1667, 1606, 1463, 1416, 1361, 764 cm–1. 1H NMR (400 MHz, CDCl3): δ = 8.26–8.28 (m, 1 H), 7.64–7.68 (m, 1 H), 7.42–7.48 (m, 2 H), 3.41 (s, 3 H), 2.29–2.36 (m, 1 H), 1.86–1.92 (m, 1 H), 1.64 (s, 3 H), 0.56 (t, J = 8.0 Hz, 3 H). 13C NMR (100 MHz, CDCl3): δ = 176.6, 164.5, 143.4, 133.9, 128.7, 127.2, 125.2, 48.3, 36.6, 28.5, 27.0, 9.4. Anal. Calcd For C13H15NO2: C, 71.87; H, 6.96; N, 6.45. Found: C, 71.68; H, 7.01; N, 6.39.