首页> 外国专利> 3 '- N - Desmethyl - 4' - O - (2 - dietilaminoetanoil) - 6 - methyl - 9A - aza - 9th - homoeritromicina, Crystalline Forms 1, 2 and 3, a process for their preparation, Pharmaceutical composition containing same and their use for the preparation of a Medicament useful for Treatment of inflammatory diseases

3 '- N - Desmethyl - 4' - O - (2 - dietilaminoetanoil) - 6 - methyl - 9A - aza - 9th - homoeritromicina, Crystalline Forms 1, 2 and 3, a process for their preparation, Pharmaceutical composition containing same and their use for the preparation of a Medicament useful for Treatment of inflammatory diseases

机译:3′-N-脱甲基-4′-O-(2-二乙胺基乙炔油)-6-甲基-9A-氮杂-第9-均铁,晶体形式1、2和3,其制备方法,包含其的药物组合物及其用于制备可用于治疗炎性疾病的药物的用途

摘要

Compound 3 '- n-destil-4' - O - (2-diethylmethylamphetamine) - 6-o-methyl-9a-aza-9a-homeritromicina a, with formula (1). The process of preparation. A pharmacist who understands this I use an effective drug to treat neutron controlled inflammation. 1. Claim 1: compound 3-n-destil-4 '- O - (2-dietelaminoyl) - 6-o-metr-9a-aza-9a-homeritromicina a, characterized by formula (1): or salt. The fifth requirement: a formula in the form of a crystal according to the fourth requirement,It is characterized in that XRPD cathode is represented by 2q angle and obtained by using a two-dimensional spectrometer radiated by copper. XRPD cathode includes 2q (2q /) angle and at least five positions selected from the group, including: 4.6, 5.6, 7.7, 9.6, 10.6, 11.0, 11.6, 11.8, 12.2, 14, The distance of grade D is 19.1, 15.9, 18.9, 18.4, 19.0, 20.5, 21.1 and 22.0 degrees respectively, and the distance of grade D is 19.1, 15.9, 11.5, 9.2, 8.4, 8.0, 7.7, 7.5, 7.2, 6.3, 5.6, 4.8, 4.7, 4.3, 4.2 and 4.0 angles (L) respectively. Item 6: according to Item 4, a formula of crystal formThis is the second form defined by the employer of XRPD with 2q angle, and obtained by a two-dimensional spectrometer with copper radiation. The employer of XRPD includes at least five 2q angles (2q / degree), selected from a group consisting of 9.1, 9.4, 10.4, 10.9, 11.5, 12.0, 13.0, 13.4 and 14.7. 15.4, 15.7, 16.5, 16.8, 18.7, 19.2, 19.5, 19.8 and 20.8 are 9.7, 9.5, 8.5, 8.1, 7.7, 7.4, 6.8, 6.6, 6.6, 6.0, 5.8, 5.6, 5, 4.6, 4.5 and 4.3 corners (troml), respectively. Item 7: according to Item 4, a formula of crystal formThis is the third form defined by the employer of XRPD with 2q angle and obtained by a two-dimensional spectrometer with copper radiation. The employer of XRPD includes 2q angle (2q / -), and there are at least five selected positions in this group, including: 5.5, 7.3, 7.9, 9.1, 9.5, 10.0, 10.5, 11.0, 11.5, 12.0, 12.6, 14.8, 15.5, 15.8, 16.6, 16.9, 18.2, 18.9, and 19.5 degrees, equivalent to 16.0, 12.1, 11.3, 9.7, 9.4, 8.9, 8.4, 8.1, 8.1, 7.7, 7.0, 6, 5.3, 5.2, 4.9, 4.7, and 4.6 corners (semicolons).
机译:化合物3'-n-destil-4'-O-(2-二乙基甲基苯丙胺)-6-邻甲基-9a-氮杂-9a-homeritromicina a,具有式(1)。准备过程。一位了解这一点的药剂师,我使用一种有效的药物来治疗中子控制的炎症。 1.权利要求1的化合物,其特征在于式(1)的化合物:3-n-destil-4′-O-(2-二乙氨基氨基)-6-邻-metr-9a-aza-9a-homeritromicina a或盐。第五要求:根据第四要求的晶体形式的公式,其特征在于,XRPD阴极由2q角表示,并且通过使用由铜辐射的二维光谱仪获得。 XRPD阴极包括2q(2q /)角和至少五个选自以下位置的位置:4.6、5.6、7.7、9.6、10.6、11.0、11.6、11.8、12.2、14,D级距离为19.1、15.9 ,分别为18.9、18.4、19.0、20.5、21.1和22.0度,并且D级距离为19.1、15.9、11.5、9.2、8.4、8.0、7.7、7.5、7.2、6.3、5.6、4.8、4.7、4.3,分别为4.2和4.0角度(L)。第6项:根据第4项,晶体形式的公式这是XRPD的雇主定义的第二种形式,具有2q角,并且是通过带有铜辐射的二维光谱仪获得的。 XRPD的雇主包括至少五个2q角度(2q /度),选自9.1、9.4、10.4、10.9、11.5、12.0、13.0、13.4和14.7。 15.4、15.7、16.5、16.8、18.7、19.2、19.5、19.8和20.8为9.7、9.5、8.5、8.1、7.7、7.4、6.8、6.6、6.6、6.0、5.8、5.6、5、4.6、4.5和4.3角(troml)。第7项:根据第4项,晶体形式的公式这是XRPD的用方定义的第三种形式,具有2q角,并且是通过带有铜辐射的二维光谱仪获得的。 XRPD的雇主包括2q角(2q /-),并且该组中至少有五个选定的职位,包括:5.5、7.3、7.9、9.1、9.5、10.0、10.5、11.0、11.5、12.0、12.6、14.8 ,15.5、15.8、16.6、16.9、18.2、18.9和19.5度,等效于16.0、12.1、11.3、19.7、9.7、9.4、8.9、8.4、8.1、8.1、7.7、7.0、6、5.3、5.2、4.9、4.7和4.6个角(分号)。

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