1988
DOI: 10.1002/chin.198815205
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ChemInform Abstract: Synthesis, Properties, and X‐Ray Analysis of 4‐Trifluoromethyl‐6‐phenyl‐2‐chloro‐3‐cyanopyridine.

Abstract: ChemInform Abstract The title compound (II), prepared from the pyridone (I) and POCl3 in the presence of DMF, reacts with nucleophiles such as (III), (V), (VII), or (IX) to give the corresponding 2-substituted pyridines (IV), (VI), (VIII), or (X). (IVf) is also obtained from (I) and the phosphorous triamide (XI). (X-ray analysis of (II): space group P21/c, Z = 8).

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“…In a typical reaction, the 2-amino-3-cyano-4-trifluoromethyl-6-phenylpyridine 2 (Narsaiah et al, 1994;Guttsait et al, 1987) was reacted with acetophenone in DMF at 120-130°C for 18 h and found several products. To improve the selectivity, the same reaction was conducted under microwave irradiation conditions using synthos 3000 microwave reactor at 540 W, 130°C and 15 bar pressure using ZnCl 2 as catalyst and on subsequent workup furnished the desired products 3 in high yields.…”
Section: Chemistrymentioning
confidence: 99%
“…In a typical reaction, the 2-amino-3-cyano-4-trifluoromethyl-6-phenylpyridine 2 (Narsaiah et al, 1994;Guttsait et al, 1987) was reacted with acetophenone in DMF at 120-130°C for 18 h and found several products. To improve the selectivity, the same reaction was conducted under microwave irradiation conditions using synthos 3000 microwave reactor at 540 W, 130°C and 15 bar pressure using ZnCl 2 as catalyst and on subsequent workup furnished the desired products 3 in high yields.…”
Section: Chemistrymentioning
confidence: 99%