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CN1231469C - 一种光学活性氨氯地平的拆分方法 - Google Patents

一种光学活性氨氯地平的拆分方法 Download PDF

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CN1231469C
CN1231469C CNB2003101193357A CN200310119335A CN1231469C CN 1231469 C CN1231469 C CN 1231469C CN B2003101193357 A CNB2003101193357 A CN B2003101193357A CN 200310119335 A CN200310119335 A CN 200310119335A CN 1231469 C CN1231469 C CN 1231469C
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amlodipine
preparation
butanone
racemic
tartrate
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CN1609102A (zh
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钟南平
赵险峰
马辉
陈玉洁
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Shijiazhuang Pharmaceutical Group Ouyi Pharma Co Ltd
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OUYI PHARMACEUTICAL CO Ltd SHIJIA ZHUANG PHARMACEUTICAL GROUP
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Priority to US10/596,209 priority patent/US7678921B2/en
Priority to PCT/CN2004/001412 priority patent/WO2005054196A1/zh
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/80Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
    • C07D211/90Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

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Abstract

本发明提供一个通过拆分消旋氨氯地平制备(S)-(-)-氨氯地平和(R)-(+)-氨氯地平对映体的方法,拆分剂是L或D-酒石酸,溶剂为2-丁酮或有机溶剂。本发明所使用的2-丁酮,沸点低,毒性小,易回收,环境污染小,适合规模生产。

Description

一种光学活性氨氯地平的拆分方法
                      技术领域
本发明涉及一种消旋体氨氯地平的化学拆分方法。
                      技术背景
氨氯地平是钙离子拮抗剂,临床用于治疗高血压和稳定型心绞痛。目前临床上应用的氨氯地平主要为消旋体,据Arrowsmiith,J.E.;etal.J.Med.Chem(1986)29;1696-1702报道,其药理活性主要成分是(S)-(-)-氨氯地平,其钙离子拮抗活性大约是(R)-(+)-氨氯地平的1000倍、消旋体的2倍;Young,J.W.,WO93/10779报道使用(S)-(-)-氨氯地平相对于使用消旋氨氯地平可以减少肢端水肿、头痛、头晕等副作用。因此采用(S)-(-)-氨氯地平治疗高血压和稳定型心绞痛具有很好的市场前景。另一对映体(R)-(+)-氨氯地平具有治疗动脉粥样硬化的活性。
氨氯地平化学结构式如下:
制备氨氯地平对映体的方法主要是拆分消旋氨氯地平。辉瑞公司的WO95/25722专利提供了一个以D或L-酒石酸为拆分剂,二甲基亚砜为溶剂,直接拆分氨氯地平得到氨氯地平对映体的方法,其不足之处是溶剂二甲基亚砜沸点高,为189℃,在生产过程中易造成溶剂不易回收的问题。Sepracor公司的WO03/035623专利描述了一种以D或L-酒石酸为拆分剂,以N,N-二甲基乙酰胺为溶剂,直接拆分氨氯地平消旋体的方法,但N,N-二甲基乙酰胺(DMAC)沸点164~166℃,沸点高不易回收,且DMAC为二类溶剂(Guidance for Industry IMPURITIES:RESIDUAL SOLVENTS,FDA,May 15,2001),毒性大,生产过程中易造成严重的污染。
                        发明内容
本发明力求寻找一种适合工业化生产氨氯地平对映体的方法。
本发明提供一个由消旋氨氯地平制备(S)-(-)-氨氯地平和(R)-(+)-氨氯地平对映体的方法。
将消旋氨氯地平和L-(+)-酒石酸溶解于含有2-丁酮的有机溶剂中,反应产生(S)-(-)-氨氯地平L-(+)-酒石酸盐的沉淀,经过过滤或离心后,再采用低级醇溶剂进行重结晶,得到上述固体,然后加入二氯甲烷,用氢氧化钠溶液中和,得到(S)-(-)-氨氯地平。
有机溶剂指的是2-丁酮或2-丁酮与助溶剂的混合溶剂。
助溶剂可以用甲醇、乙醇、正丁醇、丙酮、2-戊酮、乙醚、甲乙醚、乙酸乙酯、甲酸乙酯、二氯甲烷或氯仿。
消旋氨氯地平与L-(+)-酒石酸的摩尔比为1∶0.25-0.8。
低级醇溶剂是指乙醇、甲醇或异丙醇。
将消旋氨氯地平和D-(-)-酒石酸溶解于含有2-丁酮的有机溶剂中,反应产生(R)-(+)-氨氯地平D-(-)-酒石酸盐的沉淀,经过过滤或离心后,再采用低级醇溶剂进行重结晶,得到上述固体,然后加入二氯甲烷,用氢氧化钠溶液中和,得到(R)-(+)-氨氯地平。
有机溶剂指的是2-丁酮或2-丁酮与助溶剂的混合溶剂。
助溶剂可以用甲醇、乙醇、正丁醇、丙酮、2-戊酮、乙醚、甲乙醚、乙酸乙酯、甲酸乙酯、二氯甲烷或氯仿。
消旋氨氯地平与D-(-)-酒石酸的摩尔比为1∶0.25~0.8。
低级醇溶剂是指乙醇、甲醇或异丙醇。
氨氯地平对映体检测方法:
通过手性柱HPLC测定光学纯度,采用Ultron ES-OVM手性柱,卵类粘蛋白-15cm;流速-1ml/min;测定波长-360nm;流动相0.02mol/L磷酸氢二钠(PH7)∶乙腈=80∶20。样品溶解在乙腈∶水,50∶50,0.2mg/ml溶液。
本发明所使用的2-丁酮,沸点80℃,大量使用后容易回收。且为三类溶剂(Guidance for Industry IMPURITIES:RESIDUALSOLVENTS,FDA,May 15,2001)毒性小,环境污染小,适合规模生产。
                      具体实施方式
将消旋氨氯地平和L-(+)-酒石酸溶解于含有足够量2-丁酮的有机溶剂中,消旋氨氯地平和L-(+)-酒石酸优选摩尔比1∶0.5,反应产生(S)-(-)-氨氯地平L-(+)-酒石酸盐的沉淀,过滤,所得固体优选用乙醇重结晶,再用氢氧化钠溶液中和,得到(S)-(-)-氨氯地平。
将消旋氨氯地平和D-(-)-酒石酸溶解于含有足够量2-丁酮的有机溶剂中,消旋氨氯地平和D-(-)-酒石酸优选摩尔比1∶0.5,反应产生(R)-(+)-氨氯地平D-(-)-酒石酸盐的沉淀,过滤,所得固体优选用乙醇重结晶,再用氢氧化钠溶液中和,得到(R)-(+)-氨氯地平。
实施例一(S)-(-)-氨氯地平的制备
将5克(0.012mol)氨氯地平溶于40ml 2-丁酮中,加入溶有1.0克(0.0066mol)L-(+)-酒石酸的60ml 2-丁酮溶液,室温搅拌反应1小时,析出沉淀,过滤,用少量2-丁酮洗涤,得2.1克固体。将母液蒸馏回收2-丁酮,将所得固体在乙醇中重结晶,得(S)-(-)-氨氯地平L-(+)-酒石酸盐1.7克。
在1.7克(S)-(-)-氨氯地平L-(+)-酒石酸盐中,加入二氯甲烷18ml,2N氢氧化钠溶液10ml,搅拌反应30分钟,静置,分出有机层,加入适量无水碳酸钠干燥,过滤,用少量二氯甲烷洗涤滤饼,将滤液减压浓缩,加入适量正己烷,搅拌结晶,过滤,真空干燥过夜,得(S)-(-)-氨氯地平1.2克。利用手性柱HPLC测定其对映体过量值(ee)为99.0%,收率48%。
实施例二(R)-(+)-氨氯地平的制备
将5克(0.012mol)氨氯地平溶于40ml 2-丁酮中,加入溶有1.0克(0.0066mol)D-(-)-酒石酸的50ml 2-丁酮溶液,室温搅拌反应1小时,析出沉淀,过滤,用少量2-丁酮洗涤,得2.3克固体。将母液蒸馏回收2-丁酮,将所得固体在乙醇中重结晶,得(R)-(+)-氨氯地平D-(-)-酒石酸盐1.8克。
在1.8克(R)-(+)-氨氯地平D-(-)-酒石酸盐中,加入二氯甲烷20ml,2N氢氧化钠溶液10ml,搅拌反应30分钟,静置,分出行机层,加入适量无水碳酸钠干燥,过滤,用少量二氯甲烷洗涤滤饼,将滤液减压浓缩,加入适量正己烷,搅拌结晶,过滤,真空干燥过夜,得(R)-(+)-氨氯地平1.3克。利用手性柱HPLC测定其对映体过量值(ee)为98.8%收率52%。
实施例三(S)-(-)-氨氯地平的制备
实施方法同实施例一,将L-(+)-酒石酸的加入量改为0.5克,得(S)-(-)-氨氯地平0.9克。利用手性柱HPLC测定其对映体过量值(ee)为98.7%。
实施例四(S)-(-)-氨氯地平的制备
实施方法同实施例一,将L-(+)-酒石酸的加入量改为1.6克,得(S)-(-)-氨氯地平1.0克。利用手性柱HPLC测定其对映体过量值(ee)为95.2%。
实施例五(S)-(-)-氨氯地平的制备
实施方法同实施例一,溶剂换为下表中的助溶剂与2-丁酮的混合溶剂。
  助溶剂  助溶剂体积(V助  溶剂/V总溶剂)%   (S)-(-)-氨氯地平ee%
  水  0.1   98.5
  乙醇  1   95.2
  丙酮  1   96
  乙酸乙酯  5   94.3
  二氯甲烷  3   95.6

Claims (10)

1、一种(S)-(-)-氨氯地平的制备方法,其特征是将消旋氨氯地平和L-(+)-酒石酸溶解于含有2-丁酮的有机溶剂中,反应产生(S)-(-)-氨氯地平L-(+)-酒石酸盐的沉淀,经过过滤或离心后,再采用乙醇、甲醇或异丙醇溶剂进行重结晶,得到上述固体,然后加入二氯甲烷,用氢氧化钠溶液中和,得到(S)-(-)-氨氯地平。
2、根据权利要求1所述的(S)-(-)-氨氯地平制备方法,其特征是有机溶剂指的是2-丁酮或2-丁酮与助溶剂的混合溶剂。
3、根据权利要求2所述的(S)-(-)-氨氯地平的制备方法,其特征是助溶剂可以用甲醇、乙醇、正丁醇、丙酮、2-戊酮、乙醚、甲乙醚、乙酸乙酯、甲酸乙酯、二氯甲烷或氯仿。
4、根据权利要求1所述的(S)-(-)-氨氯地平的制备方法,其特征是消旋氨氯地平与L-(+)-酒石酸的摩尔比为1∶0.25~0.8。
5、根据权利要求4所述的(S)-(-)-氨氯地平的制备方法,其特征是消旋氨氯地平与L-(+)-酒石酸的摩尔比为1∶0.5。
6、一种(R)-(+)-氨氯地平的制备方法,其特征是将消旋氨氯地平和D-(-)-酒石酸溶解于含有2-丁酮的有机溶剂中,反应产生(R)-(+)-氨氯地平D-(-)-酒石酸盐的沉淀,经过过滤或离心后,再采用乙醇、甲醇或异丙醇溶剂进行重结晶,得到上述固体,然后加入二氯甲烷,用氢氧化钠溶液中和,得到(R)-(+)-氨氯地平。
7、根据权利要求6所述的(R)-(+)-氨氯地平的制备方法,其特征是有机溶剂指的是2-丁酮或2-丁酮与助溶剂的混合溶剂。
8、根据权利要求7所述的(R)-(+)-氨氯地平的制备方法,其特征是助溶剂可以用甲醇、乙醇、正丁醇、丙酮、2-戊酮、乙醚、甲乙醚、乙酸乙酯、甲酸乙酯、二氯甲烷或氯仿。
9、根据权利要求6所述的(R)-(+)-氨氯地平的制备方法,其特征是消旋氨氯地平与D-(-)-酒石酸的摩尔比为1∶0.25~0.8。
10、根据权利要求6所述的(R)-(+)-氨氯地平的制备方法,其特征是消旋氨氯地平与D-(-)-酒石酸的摩尔比1∶0.5。
CNB2003101193357A 2003-12-05 2003-12-05 一种光学活性氨氯地平的拆分方法 Expired - Lifetime CN1231469C (zh)

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US10/596,209 US7678921B2 (en) 2003-12-05 2004-12-03 Method for the enantiomoeric separation of optical active amlodipine
PCT/CN2004/001412 WO2005054196A1 (en) 2003-12-05 2004-12-03 A Method for the Enantiomoeric Separation of Optical Active Amlodipine

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CN100436417C (zh) * 2006-04-11 2008-11-26 石药集团中奇制药技术(石家庄)有限公司 一种光学活性氨氯地平的拆分方法
KR100868160B1 (ko) * 2007-02-14 2008-11-12 한미약품 주식회사 S-(-)-암로디핀 또는 이의 염의 제조방법 및 이에사용되는 중간체
CN111100064B (zh) * 2020-01-08 2024-01-02 湖南理工学院 一种从废液中富集、回收和拆分碱性手性药物氨氯地平的方法
CN112079770B (zh) * 2020-10-05 2024-01-02 湖南理工学院 用于高效手性拆分及母液原位再生的循环萃取和非对映体结晶耦合新方法

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GB8804630D0 (en) 1988-02-27 1988-03-30 Pfizer Ltd Preparation of r-& s-amlodipine
US6057344A (en) * 1991-11-26 2000-05-02 Sepracor, Inc. Methods for treating hypertension, and angina using optically pure (-) amlodipine
GB9405833D0 (en) 1994-03-24 1994-05-11 Pfizer Ltd Separation of the enantiomers of amlodipine
CN1100038C (zh) 2000-02-21 2003-01-29 张喜田 氨氯地平对映体的拆分
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