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Reaction of 2-amino-3-cyano-4,5,6,7-tetrahydrobenzo-[b]thiophene with ethyl acetoacetate: Novel syntheses of pyridines, pyrazoles, and their fused derivatives
✍ Scribed by Rafat M. Mohareb; Mona H. Mohamed
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 223 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.1079
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✦ Synopsis
Abstract
The reaction of 2‐amino‐3‐cyano‐4,5,6,7‐tetrahydrobenzo[b]thiophene 1 with ethyl acetoacetate 2 gave compound 3. The reactivity of the latter product toward a variety of chemical reagents was studied to give fused thiophene derivatives of potential pharmaceutical interest. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:518–527, 2001
📜 SIMILAR VOLUMES
## Abstract The reaction of 2‐amino‐3‐cyano‐4,5,6,7‐tetrahydrobenzo[b]thiophene (**1**) with diethyl malonate (**2**) gave two products: **3** and **4**. The reactivity of **3** toward a variety of chemical reagents was studied to give azoles, azines, and their fused derivatives. © 2001 John Wiley
## Abstract 2‐Amino‐3‐cyano‐4,5,6,7‐tetrahydrobenzo[__b__]thiophene **1a** or 2‐amino‐3‐cyano‐4,7‐di‐ phenyl‐5‐methyl‐4__H__‐pyrano[2,3‐__c__]pyrazole **2a** reacted with phenylisocyanate in dry pyridine to give 2‐(3‐phenylureido)‐3‐cyanobenzo[b]thiophene **1b** or 2‐disubstituted amino‐3‐cyanopyra