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2006•Acta Crystallographica Section E Structure Reports OnlineRequires access

Ethyl 1-(1,2,3-benzothiadiazol-7-ylcarbonyl)piperidine-4-carboxylate

Jian-Zhuang Zhao, Lili Bao, Zhijin Fan, Haibin Song, Xiufeng Liu

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Abstract

The title compound, C15H17N3O3S, a potent new plant elicitor, was synthesized by reaction between 1,2,3-benzothia­diazole-7-carbonyl chloride and ethyl piperidine-4-carboxyl­ate. The piperidine ring adopts a chair conformation. Weak inter­molecular C—H⋯O hydrogen bonds stabilize the crystal packing.

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What this paper is about

The title compound, C15H17N3O3S, a potent new plant elicitor, was synthesized by reaction between 1,2,3-benzothia­diazole-7-carbonyl chloride and ethyl piperidine-4-carboxyl­ate. The piperidine ring adopts a chair conformation. Weak inter­molecular C—H⋯O hydrogen bonds stabilize the crystal packing.

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Available abstract

The title compound, C15H17N3O3S, a potent new plant elicitor, was synthesized by reaction between 1,2,3-benzothia­diazole-7-carbonyl chloride and ethyl piperidine-4-carboxyl­ate. The piperidine ring adopts a chair conformation. Weak inter­molecular C—H⋯O hydrogen bonds stabilize the crystal packing.

Key concepts: Piperidine, Cyclohexane conformation, Carboxylate, Ring (chemistry), Hydrogen bond, Chemistry, Chloride, Crystal structure

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