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Total synthesis and analgesic activity of 6-fluoroindan-1-carboxylic acid

机译:6-氟茚满-1-羧酸的全合成和止痛活性

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6-fluoroindan-1-carboxylic acid (4) was conveniently synthesised from 3-fluorobenzaldehyde in six steps. The structure of this new compound and three other intermediates, 3-fluorophenylcyanoethylacrylate (1), 3-fluorophenyl succinic acid (2) and 6-fluoro-3-oxo-indan-1-carboxylic acid (3) was elucidated by comprehensive spectral data analyses. The analgesic activity of compounds 3 and 4 was assessed by the acetic acid induced writhing in Swiss albino mice. (c) 2008 Elsevier Ltd. All rights reserved.
机译:从6-氟苯甲醛分六步方便地合成6-氟茚满-1-羧酸(4)。通过综合光谱数据阐明了该新化合物和其他三种中间体的结构,即3-氟苯基氰基乙基丙烯酸酯(1),3-氟苯基琥珀酸(2)和6-氟-3-氧代-茚满-1-羧酸(3)。分析。通过乙酸在白化病小鼠中引起的扭体作用来评估化合物3和4的镇痛活性。 (c)2008 Elsevier Ltd.保留所有权利。

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