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SUPPORTING INFORMATIONSynthesis and Biological Activity of (2-Substituted-4-methylthiazol-5-yl)(4-substituted piperazin-1-yl)methanone Derivatives

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Journal of the Korean Chemical Society 2014, Vol. 58, No. 1

Printed in the Republic of Korea http://dx.doi.org/10.5012/jkcs.2014.58.1.1

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SUPPORTING INFORMATION

Synthesis and Biological Activity of (2-Substituted-4-methylthiazol-5-yl) (4-substituted piperazin-1-yl)methanone Derivatives

Pravin C. Mhaske*, Shivaji H. Shelke

, Hemant N. Raundal

, and Rahul P. Jadhav

Post Graduate Department of Chemistry, S. P. Mandali’s Sir Parashurambahu College,

Tilak Road, Pune, India 411 030, (Affiliated to University of Pune).

*E-mail: [email protected]

Department of Chemistry, HPT Arts and RYK Science College, Nashik India-422 005 (Received September 2, 2013; Accepted December 17, 2013)

Figure S1. 1H NMR (CDCl3, 300 MHz) of (4-(2,4-dichlorophenyl)piperazin-1-yl)(2,4-dimethylthiazol-5-yl)methanone (5a).

Spectral data of representative compounds

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Journal of the Korean Chemical Society 2 Pravin C. Mhaskea, Shivaji H. Shelke, Hemant N. Raundal, and Rahul P. Jadhav

Figure S2. 1H NMR (CDCl3, 300 MHz) of (4-(2,4-dichlorophenyl)piperazin-1-yl)(4-methyl-2-phenylthiazol-5-yl)methanone (5b).

Figure S3. 1H NMR (CDCl3, 300 MHz) of (2-(4-fluorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5d).

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Synthesis and Biological Activity of (2-Substituted-4-methylthiazol-5-yl)(4-substituted piperazin-1-yl)methanone Derivatives 3

2014, Vol. 58, No. 1

Figure S5. 1H NMR (CDCl3, 300 MHz) of (2-(2,4-dichlorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5e).

Figure S4. 13C NMR (CDCl3, 75 MHz) of (2-(4-fluorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5d).

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Journal of the Korean Chemical Society 4 Pravin C. Mhaskea, Shivaji H. Shelke, Hemant N. Raundal, and Rahul P. Jadhav

Figure S8. 13C NMR (CDCl3, 75 MHz) of (2-(2,4-dichlorobenzyl)-4-methylthiazol-5-yl)(4-(4-chlorobenzyl)piperazin-1-yl)methanone (5k).

Figure S7. 13C NMR (CDCl3, 75 MHz) of (4-(4-chlorobenzyl)piperazin-1-yl)(4-methyl-2-phenylthiazol-5-yl)methanone (5h).

Figure S6. 13C NMR (CDCl3, 75 MHz) of (2-(2,4-dichlorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5e).

수치

Figure S1.  1 H NMR (CDCl 3 , 300 MHz) of (4-(2,4-dichlorophenyl)piperazin-1-yl)(2,4-dimethylthiazol-5-yl)methanone (5a).
Figure S3.  1 H NMR (CDCl 3 , 300 MHz) of (2-(4-fluorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5d).
Figure S5.  1 H NMR (CDCl 3 , 300 MHz) of (2-(2,4-dichlorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5e).
Figure S6.  13 C NMR (CDCl 3 , 75 MHz) of (2-(2,4-dichlorobenzyl)-4-methylthiazol-5-yl)(4-(2,4-dichlorophenyl)piperazin-1-yl)methanone (5e).

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