2005
DOI: 10.1002/jlcr.1032
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Synthesis of carbon‐14 analogue of N‐(1‐methyl‐2‐oxo‐5‐phenyl‐2,3‐dihydro‐1H‐benzo[e][1,4]diazepin‐3‐yl)‐benzamide‐[carboxyl‐14C] as CCK‐A antagonist

Abstract: N‐(1‐methyl‐2‐oxo‐5‐phenyl‐2,3‐dihydro‐1H‐benzo[e][1,4]diazepin‐3‐yl)‐benzamide‐[carboxyl‐14C] has been synthesized from benzonitrile‐[cyano‐14C]. Copyright © 2005 John Wiley & Sons, Ltd.

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Cited by 12 publications
(4 citation statements)
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“…In this approach, according to the synthetic pathway shown in Scheme , potassium [ 14 C]‐thio‐cyanate 5 was obtained quantitatively via the reaction between potassium [ 14 C] cyanide 4 and sulfur in acetone 12, 13…”
Section: Resultsmentioning
confidence: 99%
“…In this approach, according to the synthetic pathway shown in Scheme , potassium [ 14 C]‐thio‐cyanate 5 was obtained quantitatively via the reaction between potassium [ 14 C] cyanide 4 and sulfur in acetone 12, 13…”
Section: Resultsmentioning
confidence: 99%
“…Synthesis of 14 C labelled anthranilic acid (3) has been reported in the literature 1,14,15 which requires special equipment for handling. In all reported methods more than one equivalent of 14 C precursor was used.…”
Section: Introductionmentioning
confidence: 99%
“…4 In this paper, the synthesis 7 Subsequent alkylation of compound 7 with ethyl iodide and oxidation of the product with manganese dioxide and further oxidation of the latter product with alkaline solution of silver nitrate gave [2-14 C]-2-ethylthio-1-benzylimidazole-5-carboxylic acid 8.…”
Section: Introductionmentioning
confidence: 99%