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公开(公告)号:US08648189B2
公开(公告)日:2014-02-11
申请号:US13577441
申请日:2011-02-10
申请人: Hubert Sturm , Dominic De Souza , Kerstin Knepper , Martin Albert
发明人: Hubert Sturm , Dominic De Souza , Kerstin Knepper , Martin Albert
IPC分类号: C07D419/10 , C07D419/14 , C07D333/22
CPC分类号: C07D413/14 , C07D265/32 , C07D333/38 , C07D409/12 , C07D413/12
摘要: The present invention relates to the use of a compound having the formula (II) for the preparation of a compound having the formula (V). Methods of preparing the compound having the formula (V) using the compound having the formula (II) are also described. Individual reaction steps as well as intermediates are additionally claimed.
摘要翻译: 本发明涉及具有式(II)的化合物在制备具有式(V)的化合物中的用途。 还描述了使用具有式(II)的化合物制备具有式(V)的化合物的方法。 单独的反应步骤以及中间体也被要求保护。
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公开(公告)号:US08481758B2
公开(公告)日:2013-07-09
申请号:US12500669
申请日:2009-07-10
IPC分类号: C07D307/93 , C07C69/76
CPC分类号: C07C405/00 , C07D307/935
摘要: The present invention relates to an improved process for the production of prostaglandins and prostaglandin analogs. In particular, this invention relates to the production of prostaglandins of the PGF2α-series, including latanoprost, travoprost, and bimatoprost, which are active pharmaceutical ingredients used for the reduction of elevated intra-ocular pressure in patients with glaucoma and ocular hypertension.
摘要翻译: 本发明涉及前列腺素和前列腺素类似物的生产改进方法。 特别地,本发明涉及PGF2α系列前列腺素的生产,包括拉坦前列素,曲伏前列素和比马前列素,它们是用于降低青光眼和高眼压患者眼内压升高的活性药物成分。
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公开(公告)号:US20130184457A1
公开(公告)日:2013-07-18
申请号:US13577441
申请日:2011-02-10
申请人: Hubert Sturm , Dominic De Souza , Kerstin Knepper , Martin Albert
发明人: Hubert Sturm , Dominic De Souza , Kerstin Knepper , Martin Albert
IPC分类号: C07D413/14 , C07D413/12 , C07D409/12 , C07D333/38
CPC分类号: C07D413/14 , C07D265/32 , C07D333/38 , C07D409/12 , C07D413/12
摘要: The present invention relates to the use of a compound having the formula (II) for the preparation of a compound having the formula (V). Methods of preparing the compound having the formula (V) using the compound having the formula (II) are also described. Individual reaction steps as well as intermediates are additionally claimed.
摘要翻译: 本发明涉及具有式(II)的化合物在制备具有式(V)的化合物中的用途。 还描述了使用具有式(II)的化合物制备具有式(V)的化合物的方法。 单独的反应步骤以及中间体也被要求保护。
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公开(公告)号:US09040539B2
公开(公告)日:2015-05-26
申请号:US13697806
申请日:2011-05-18
申请人: Michael Oberhuber , Joerg Salchenegger , Dominic De Souza , Martin Albert , Thorsten Wilhelm , Martin Langner , Hubert Sturm , Hans-Peter Spitzenstaetter
发明人: Michael Oberhuber , Joerg Salchenegger , Dominic De Souza , Martin Albert , Thorsten Wilhelm , Martin Langner , Hubert Sturm , Hans-Peter Spitzenstaetter
IPC分类号: A61K31/496 , C07D405/14 , C07D295/155 , C07D405/06
CPC分类号: C07D295/155 , C07D405/06 , C07D405/14
摘要: A process for the preparation of a chiral compound, in particular posaconazole, wherein the process comprises mixing and reacting the compounds of formula (I) Y3—NH2; of formula (IIa) 0=C═N—Y0 and/or of formula (IIb) and of formula (III) in a solvent in any order to obtain a reaction mixture containing a chiral compound of formula (IV) and/or formula (V).
摘要翻译: 一种制备手性化合物,特别是泊沙康唑的方法,其中该方法包括将式(I)Y 3 -NH 2的化合物混合并反应; 的式(IIa)0 = C = N-Y0和/或式(IIb)和式(III)的化合物在溶剂中以任何顺序获得含有式(IV)和/或式 (V)。
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公开(公告)号:US20130210833A1
公开(公告)日:2013-08-15
申请号:US13697806
申请日:2011-05-18
申请人: Michael Oberhuber , Joerg Salchenegger , Dominic De Souza , Martin Albert , Thorsten Wilhelm , Martin Langner , Hubert Sturm , Hans-Peter Spitzenstaetter
发明人: Michael Oberhuber , Joerg Salchenegger , Dominic De Souza , Martin Albert , Thorsten Wilhelm , Martin Langner , Hubert Sturm , Hans-Peter Spitzenstaetter
IPC分类号: C07D295/155
CPC分类号: C07D295/155 , C07D405/06 , C07D405/14
摘要: A process for the preparation of a chiral compound, in particular posaconazole, wherein the process comprises mixing and reacting the compounds of formula (I) Y3—NH2; of formula (IIa) 0=C═N—Y0 and/or of formula (IIb) and of formula (III) in a solvent in any order to obtain a reaction mixture containing a chiral compound of formula (IV) and/or formula (V).
摘要翻译: 一种制备手性化合物,特别是泊沙康唑的方法,其中该方法包括将式(I)Y 3 -NH 2的化合物混合并反应; 式(IIa)的化合物0 = C = N-Y0和/或式(IIb)和式(III)的化合物在溶剂中以任何顺序得到含有式(Ⅳ)和/或式 (V)。
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公开(公告)号:US20110178340A1
公开(公告)日:2011-07-21
申请号:US12999112
申请日:2009-06-10
申请人: Dominic De Souza , Martin Albert , Hubert Sturm
发明人: Dominic De Souza , Martin Albert , Hubert Sturm
IPC分类号: C07C405/00
CPC分类号: C07C231/24 , C07C231/12 , C07C235/34 , C07C2601/08
摘要: The present invention relates to a process for the purification of crude bimatoprost to obtain pure bimatoprost comprising a chromatography, preferably a chromatography using an achiral stationary phase and an eluent comprising an alcohol and an apolar solvent; and crystallisation of the product obtained the chromatography to obtain pure bimatoprost.
摘要翻译: 本发明涉及纯化比马前列素以获得纯比马前列素的方法,其包括色谱法,优选使用非手性固定相的色谱法和包含醇和非极性溶剂的洗脱液; 并将得到的产物进行结晶,得到纯比马前列素。
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公开(公告)号:US08772544B2
公开(公告)日:2014-07-08
申请号:US12999112
申请日:2009-06-10
申请人: Dominic De Souza , Martin Albert , Hubert Sturm
发明人: Dominic De Souza , Martin Albert , Hubert Sturm
IPC分类号: C07C233/05
CPC分类号: C07C231/24 , C07C231/12 , C07C235/34 , C07C2601/08
摘要: The present invention relates to a process for the purification of crude bimatoprost to obtain pure bimatoprost comprising a chromatography, preferably a chromatography using an achiral stationary phase and an eluent comprising an alcohol and an apolar solvent; and crystallization of the product obtained the chromatography to obtain pure bimatoprost.
摘要翻译: 本发明涉及纯化比马前列素以获得纯比马前列素的方法,其包括色谱法,优选使用非手性固定相的色谱法和包含醇和非极性溶剂的洗脱液; 并使产物结晶得到纯化比马前列素。
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公开(公告)号:US09221771B2
公开(公告)日:2015-12-29
申请号:US14111365
申请日:2012-04-11
申请人: Hubert Sturm , Kerstin Knepper
发明人: Hubert Sturm , Kerstin Knepper
IPC分类号: C07D265/30 , C07D265/32 , C07D413/10 , C07D417/14 , C07D487/18
CPC分类号: C07D265/30 , C07D265/32 , C07D413/10 , C07D417/14 , C07D487/18
摘要: The present invention relates to methods for the preparation of a compound having the formula (X). Individual reaction steps as well as intermediates are additionally claimed.
摘要翻译: 本发明涉及制备具有式(X)的化合物的方法。 单独的反应步骤以及中间体也被要求保护。
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公开(公告)号:US20140329989A1
公开(公告)日:2014-11-06
申请号:US14241472
申请日:2012-09-07
申请人: Roland Barth , Kerstin Knepper , Hubert Sturm
发明人: Roland Barth , Kerstin Knepper , Hubert Sturm
IPC分类号: C07F9/653 , C07K7/64 , C07D417/12 , C07D261/08 , C07D413/12
CPC分类号: C07K7/64 , C07D261/08 , C07D413/12 , C07D413/14 , C07D417/12 , C07F9/653 , C07K7/56
摘要: The present invention relates to the preparation of compounds, in particular to the preparation of compounds of formula (I), which may be used with a compound of formula (VI), or a salt thereof as intermediates for the preparation of antifungal agents, preferably micafungin (MICA) or a salt thereof.
摘要翻译: 本发明涉及化合物的制备,特别是制备式(I)化合物,其可与式(VI)化合物或其盐一起用作制备抗真菌剂的中间体,优选 米卡芬净(MICA)或其盐。
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公开(公告)号:US20140213784A1
公开(公告)日:2014-07-31
申请号:US14111365
申请日:2012-04-11
申请人: Hubert Sturm , Kerstin Knepper
发明人: Hubert Sturm , Kerstin Knepper
IPC分类号: C07D413/10 , C07D417/14 , C07D487/18 , C07D265/30 , C07D265/32
CPC分类号: C07D265/30 , C07D265/32 , C07D413/10 , C07D417/14 , C07D487/18
摘要: The present invention relates to methods for the preparation of a compound having the formula (X). Individual reaction steps as well as intermediates are additionally claimed.
摘要翻译: 本发明涉及制备具有式(X)的化合物的方法。 单独的反应步骤以及中间体也被要求保护。
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