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1-(α-萘甲基)-2甲基-6,7-二甲氧基-1,2,3,4-四氢异喹啉盐酸盐的HPLC手性拆分法及半制备
引用本文:王义明,罗国安,彭健斌,詹少卿,刘子列,林炳承. 1-(α-萘甲基)-2甲基-6,7-二甲氧基-1,2,3,4-四氢异喹啉盐酸盐的HPLC手性拆分法及半制备[J]. 药学学报, 1995, 30(11): 854-857
作者姓名:王义明  罗国安  彭健斌  詹少卿  刘子列  林炳承
作者单位:清华大学化学系,北京 100084;1.中美天津史克制药有限公司,2.南通第一人民医院,3.南京师范大学,4.中科院大连化学物理所
摘    要:1-(α-Naphthylmethy)-2-methyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolinehydrochloride (code No, 86040)is a new kind of calcium antagonist. It has(+)and(一)enantiomers.Accordingly .the resolution and quantification of these two enantiomers have received agreat deal of attention,In this report the application of direct HPLC separation and semipreparation tothe determination of the enantiomeric composition of the new drug are described. All analysis andsemipreparation were performed with 25 cm×4. 6 mm i.d, 25 cm×8 mm i,d.and 30 cm×8 mmi.d. stainless steel column packed with a chiral β-cycledextrin bonded phase. Detection wavelengthwas 284 nm, The optimal composition of the mobile phase was EtOH─pH 4.0 phosphate buffer(35:65) at flow rate of 0. 3 ml·min-1 for analysis and l.0 ml·min-1 for semipreparation. Theseparation factor of the enantiomers was l.25. Purity of the semipreparation was 8l.4%,Quantityof semipreparation was 1 mg. This procedure was simple ,rapid and gave good resolution,The effectsof the composition of mobile phase, pH value, flow rate and column temperature on the resolution hadbeen sudied.

关 键 词:1-(α-萘甲基)-2-甲基-6  7-二甲氧基-1  4-四氢异喹啉盐酸盐  β-CD手性固定相  HPLC拆分  半制备
收稿时间:1995-03-15

ENANTIOMER SEPARATION AND SEMIPREPARATION OF 1-(α-NAPHTHYLMETHY)-2-METHYL-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE BY HPLC METHOD
YM Wang,GA Luo,JB Peng,SQ Zhan,ZL Liu and BC Lin. ENANTIOMER SEPARATION AND SEMIPREPARATION OF 1-(α-NAPHTHYLMETHY)-2-METHYL-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE BY HPLC METHOD[J]. Acta pharmaceutica Sinica, 1995, 30(11): 854-857
Authors:YM Wang  GA Luo  JB Peng  SQ Zhan  ZL Liu  BC Lin
Abstract:
Keywords:Chiral β-CD stationary phase  Enantiomer separation by HPLC  1-(α-Naphthylmethy )-2-methyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
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