2-(1-Methyl-1H-indol-3-ylmethylene)-1-aza-bicyclo[2.2.2] octan-3-one: Acid-catalyzed isomerization of the Z isomer to the E isomer

被引:0
作者
Vijayakumar N. Sonar
Sean Parkin
Peter A. Crooks
机构
[1] College of Pharmacy,Division of Pharmaceutical Sciences
[2] University of Kentucky,Department of Chemistry
[3] University of Kentucky,undefined
来源
Journal of Chemical Crystallography | 2004年 / 34卷
关键词
Heterocycle; indole; quinuclidinone; synthesis; single crystal x-ray structure;
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摘要
Crystals of (Z)-2-(1-methyl-1H-indol-3-ylmethylene)-1-aza-bicyclo[2.2.2]octan-3-one (I) were obtained from a condensation reaction of 1-methyl-1H-indole-3-carboxaldehyde with 1-aza-bicyclo[2.2.2]octan-3-one and subsequent crystallization of the product from methanol. The isomeric (E)-2-(1-methyl-1H-indol-3-ylmethylene)-1-aza-bicyclo[2.2.2] octan-3-one hydrochloride (II) was obtained by treating a methanolic solution of I with a 1M solution of hydrogen chloride diethyl ether, followed by crystallization of resultant product from methanol. Crystal data: I, is monoclinic, P21, a = 5.7440(10), b = 11.102(2), c = 10.708(2) Å, β = 91.751(10)°, and V = 682.5(2) Å3 with Z = 2, for Dcal= 1.296 mg/m3 and II, is monoclinic, P21/c, a = 8.8510(2), b = 17.4990(5), c = 20.4300(5) Å, β = 101.3620(12)°, V = 3102.26(14) with Z = 8, for Dcal= 1.316 mg/m3.
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页码:239 / 244
页数:5
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