JP2004509062A5 - - Google Patents

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Publication number
JP2004509062A5
JP2004509062A5 JP2001563121A JP2001563121A JP2004509062A5 JP 2004509062 A5 JP2004509062 A5 JP 2004509062A5 JP 2001563121 A JP2001563121 A JP 2001563121A JP 2001563121 A JP2001563121 A JP 2001563121A JP 2004509062 A5 JP2004509062 A5 JP 2004509062A5
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JP
Japan
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2001563121A
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Japanese (ja)
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JP2004509062A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2000/033843 external-priority patent/WO2001064224A1/en
Publication of JP2004509062A publication Critical patent/JP2004509062A/ja
Publication of JP2004509062A5 publication Critical patent/JP2004509062A5/ja
Withdrawn legal-status Critical Current

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JP2001563121A 2000-02-29 2000-12-15 クラリスロマイシンおよびクラリスロマイシン中間体、本質的にオキシムを含まないクラリスロマイシン、およびそれを含んで成る医薬組成物を調製するための方法 Withdrawn JP2004509062A (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US18588800P 2000-02-29 2000-02-29
US18912000P 2000-03-14 2000-03-14
US21323900P 2000-06-22 2000-06-22
PCT/US2000/033843 WO2001064224A1 (en) 2000-02-29 2000-12-15 Processes for preparing clarithromycin and clarithromycin intermediate, essentially oxime-free clarithromycin, and pharmaceutical composition comprising the same

Publications (2)

Publication Number Publication Date
JP2004509062A JP2004509062A (ja) 2004-03-25
JP2004509062A5 true JP2004509062A5 (enExample) 2005-12-22

Family

ID=27392028

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001563121A Withdrawn JP2004509062A (ja) 2000-02-29 2000-12-15 クラリスロマイシンおよびクラリスロマイシン中間体、本質的にオキシムを含まないクラリスロマイシン、およびそれを含んで成る医薬組成物を調製するための方法

Country Status (15)

Country Link
US (3) US6617436B2 (enExample)
EP (1) EP1313486A1 (enExample)
JP (1) JP2004509062A (enExample)
KR (1) KR20030047873A (enExample)
AU (2) AU2001225787C1 (enExample)
CA (1) CA2401571A1 (enExample)
CZ (1) CZ20023167A3 (enExample)
HR (1) HRP20020709A2 (enExample)
HU (1) HUP0302466A2 (enExample)
IL (1) IL151496A0 (enExample)
IS (1) IS6531A (enExample)
PL (1) PL366021A1 (enExample)
SK (1) SK13722002A3 (enExample)
WO (1) WO2001064224A1 (enExample)
YU (1) YU64202A (enExample)

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CN102417532A (zh) * 2011-12-20 2012-04-18 浙江国邦药业有限公司 一种泰利霉素关键中间体5-德胺糖基-6-o-甲基红霉素的合成方法
CN102718821B (zh) * 2012-06-27 2014-12-03 浙江国邦药业有限公司 一种克拉霉素合成过程中甲基化反应以及甲基化试剂的回收套用方法
CN103880901A (zh) * 2012-12-23 2014-06-25 菏泽市方明制药有限公司 一种克拉霉素中间甲化物的制备方法
CN106905204B (zh) * 2017-02-24 2018-07-20 杭州新桂实业有限公司 一种克拉霉素合成过程中甲基化反应溶剂的回收套用方法
CN108117573A (zh) * 2017-12-26 2018-06-05 宁夏启元药业有限公司 4"-o-(三甲基硅)红霉素a 9-o-(1-乙氧基-1-甲基乙基)肟的合成方法

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