Synlett 2015; 26(09): 1213-1216
DOI: 10.1055/s-0034-1380573
letter
© Georg Thieme Verlag Stuttgart · New York

Copper-Catalyzed Oxidative ipso-Cyclization of N-(p-Methoxyaryl)propiolamides with Disulfides and Water Leading to 3-(Arylthio)-1-azaspiro[4.5]deca-3,6,9-triene-2,8-diones

Peng-Cheng Qian
a   State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. of China   Email: jhli@hnu.edu.cn   Email: srj0731@hnu.edu.cn
b   College of Chemistry and Materials engineering, Wenzhou University, Wenzhou, 325035, P. R. of China
,
Yu Liu
a   State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. of China   Email: jhli@hnu.edu.cn   Email: srj0731@hnu.edu.cn
,
Ren-Jie Song*
a   State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. of China   Email: jhli@hnu.edu.cn   Email: srj0731@hnu.edu.cn
,
Jian-Nan Xiang
a   State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. of China   Email: jhli@hnu.edu.cn   Email: srj0731@hnu.edu.cn
,
Jin-Heng Li*
a   State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, P. R. of China   Email: jhli@hnu.edu.cn   Email: srj0731@hnu.edu.cn
› Author Affiliations
Further Information

Publication History

Received: 26 February 2015

Accepted after revision: 23 March 2015

Publication Date:
23 April 2015 (online)


Abstract

A new copper-catalyzed oxidative ipso-cyclization of N-(p-methoxyaryl)propiolamides with disulfides for the synthesis of 3-(arylthio)-1-azaspiro[4.5]deca-3,6,9-triene-2,8-diones has been developed. This method proceeds via sequential oxidative C–S bond formation, ipso-cyclization, and dearomatization and provides a new facile oxidative strategy to assemble the target products using an inexpensive catalytic system comprising copper(II) chloride and molecular oxygen.

Supporting Information

 
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  • 8 Copper-Catalyzed Oxidative ispo-Cyclization to 3-(Arylthio)-1-azaspiro[4.5]deca-3,6,9-triene-2,8-diones; Typical Procedure To a Schlenk tube were added N-(p-methoxyaryl)propiolamide 1a (0.2 mmol), 1,2-diphenyldisulfane (2a, 1.5 equiv), H2O (2 equiv), CuCl2 (10 mol%), and DMF (anhydrous; 2 mL). Then the tube was charged with oxygen and was stirred at 100 °C for 24 h until complete consumption of starting material as monitored by TLC and/or GC–MS analysis. After the reaction was finished, the reaction mixture was washed with brine. The aqueous phase was re-extracted with EtOAc. The combined organic extracts were dried over Na2SO4, concentrated in vacuum, and the resulting residue was purified by silica gel column chromatography (hexane–EtOAc) to afford the desired product 3aa. 1-Methyl-4-phenyl-3-(phenylthio)-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione (3aa) Yellow solid; mp 157.6–159.4 °C (uncorrected). 1H NMR (400 MHz, CDCl3): δ = 7.29–7.17 (m, 10 H), 6.54 (d, J = 8.8 Hz, 2H), 6.47 (d, J = 8.8 Hz, 2 H), 2.89 (s, 3 H). 13C NMR (100 MHz, CDCl3): δ = 183.9, 167.6, 152.7, 145.1, 133.1, 132.1, 131.6, 130.9, 130.6, 129.6, 128.9, 128.2, 128.0, 127.4, 67.7, 26.2. IR (KBr): 1700, 1664 cm–1. ESI-HRMS: m/z calcd for C22H17NO2S [M + H]+: 360.1053; found: 360.1058