Knowing When To Stop-Trapping Metastable Polymorphs in Mechanochemical Reactions

被引:32
|
作者
Kulla, Hannes [1 ,2 ]
Greiser, Sebastian [1 ]
Benemann, Sigrid [1 ]
Rademann, Klaus [2 ]
Emmerlingt, Franziska [1 ]
机构
[1] BAM Fed Inst Mat Res & Testing, Richard Willstatter Str 11, D-12489 Berlin, Germany
[2] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
关键词
X-RAY-DIFFRACTION; ACTIVE PHARMACEUTICAL INGREDIENTS; IN-SITU; REAL-TIME; COCRYSTAL FORMATION; CARBOXYLIC-ACIDS; SYSTEMATIC CONSTRUCTION; RELATIVE STABILITY; MILLING REACTIONS; CO-CRYSTAL;
D O I
10.1021/acs.cgd.6b01572
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cocrystal formation of pyrazinamide (PZA) with malonic acid (MA) was studied in situ. The mechanochemical reaction proceeds via conversion of a crystalline intermediate (PZA:MA II) into the thermodynamically more stable form (PZA:MA I) upon further grinding. The information derived from in situ powder X-ray diffraction (PXRD) enabled the isolation of this new metastable polymorph. On the basis of the PXRD data, the crystal structure of the 1:1 cocrystal PZA:MA II was solved. The polymorphs were further characterized and compared by Raman spectroscopy, solid-state NMR spectroscopy, differential thermal analysis/thermogravimetric analysis, and scanning electron microscopy. Our study demonstrates how monitoring mechanochemical reactions by in situ PXRD can direct the discovery and isolation of even short-lived intermediates not yet accessed by conventional methods.
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页码:1190 / 1196
页数:7
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