Flavin M T, Rizzo J D, Khilevich A, Kucherenko A, Sheinkman A K, Vilaychack V, Lin L, Chen W, Greenwood E M, Pengsuparp T, Pezzuto J M, Hughes S H, Flavin T M, Cibulski M, Boulanger W A, Shone R L, Xu Z Q
MediChem Research, Inc., Lemont, Illinois 60439, USA.
J Med Chem. 1996 Mar 15;39(6):1303-13. doi: 10.1021/jm950797i.
The anti-HIV agent (+/-)-calanolide A (1) has been synthesized in a five-step approach starting with phloroglucinol [-->5-->6-->11-->18-->(+/-)-1], which includes Pechmann reaction, Friedel-Crafts acylation, chromenylation with 4,4-dimethoxy-2-methylbutan-2-ol, cyclization, and Luche reduction. Cyclization of chromene 11 to chromanone 18 was achieved by employing either acetaldehyde diethyl acetal or paraldehyde in the presence of trifluoroacetic acid and pyridine or PPTS. Luche reduction of chromanone 18 at lower temperature preferably yielded (+/-)-1. Reduction of chromone 12, synthesized by Kostanecki-Robinson reaction from chromene 11, failed to afford (+/-)-1. The synthetic (+/-)-1 has been chromatographically resolved into its optically active forms, (+)- and (-)-1. The anti-HIV activities for synthetic (+/-)-1, as well as resultant (+)- and (-)-1, have been determined. Only (+)-1 accounted for anti-HIV activity, which was similar to the data reported for the natural product, and (-)-1 was inactive.
抗HIV药物(±)-卡拉诺内酯A(1)已通过一种五步方法合成,该方法以间苯三酚为起始原料[→5→6→11→18→(±)-1],包括Pechmann反应、傅克酰基化反应、用4,4-二甲氧基-2-甲基丁-2-醇进行苯并二氢吡喃化反应、环化反应和卢切还原反应。在三氟乙酸和吡啶或PPTS存在下,使用乙醛二乙缩醛或三聚甲醛可实现苯并二氢吡喃11环化为苯并二氢吡喃酮18。在较低温度下对苯并二氢吡喃酮18进行卢切还原反应,优选得到(±)-1。由苯并二氢吡喃11通过科斯塔内茨基-罗宾逊反应合成的苯并二氢吡喃酮12的还原反应未能得到(±)-1。合成的(±)-1已通过色谱法拆分为其旋光活性形式,即(+)-和(-)-1。已测定了合成的(±)-1以及所得的(+)-和(-)-1的抗HIV活性。只有(+)-1具有抗HIV活性,这与天然产物报道的数据相似,而(-)-1无活性。