异烟肼衍生物与丁-2-酮和丙-2-酮的一系列共晶的合成和表征。

IF 0.7 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
Matthew Clarke Scheepers, Andreas Lemmerer
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引用次数: 0

摘要

通过将异烟肼与丁-2-酮(前者)或丙酮(后者)反应,合成了四个含有N’-(丁-2-亚基)吡啶-4-碳酰肼的共晶(izbt)和一个含有N‘-异亚丙基eisonicotinohydride(izact)的共晶。用于合成izbt共晶的共形成物为2,4-二羟基苯甲酸、2,5-二羟基苯乙酸、2-氯-4-硝基苯甲酸和1-萘甲酸。1-萘甲酸也与izact一起使用以形成共结晶。1:1共晶为:N’-(丁-2-亚基)吡啶-4-碳酰肼-1-萘甲酸(izbt-1nta)、C10H13N3O·C11H8O2、N’-,N'-(丁-2-亚基)吡啶-4-碳酰肼-2-氯-4-硝基苯甲酸(izbt-2c4n),C10H13N3O·C7H4ClNO4,和N'-。将含有izbt的共晶与本文或剑桥结构数据库(CSD)中报道的含有与izact相同(或相似)共形成物的共晶进行比较。尽管具有相同的氢键基序,但大多数共晶显示出不同的堆积。用单晶X射线衍射(SC-XRD)、粉末X射线衍射法(PXRD)和差示扫描量热法(DSC)对共晶进行了表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The synthesis and characterization of a series of cocrystals of an isoniazid derivative with butan-2-one and propan-2-one.

Four cocrystals containing N'-(butan-2-ylidene)pyridine-4-carbohydrazide (izbt) and one cocrystal containing N'-isopropylideneisonicotinohydrazide (izact) were synthesized by reacting isoniazid with either butan-2-one (for the former) or acetone (for the latter). The coformers used to synthesize the izbt cocrystals were 2,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, 2-chloro-4-nitrobenzoic acid and 1-naphthoic acid. 1-Naphthoic acid was also used with izact to form a cocrystal. The 1:1 cocrystals are: N'-(butan-2-ylidene)pyridine-4-carbohydrazide-1-naphthoic acid (izbt-1nta), C10H13N3O·C11H8O2, N'-(butan-2-ylidene)pyridine-4-carbohydrazide-2,4-dihydroxybenzoic acid (izbt-2,4-dhba), C10H13N3O·C7H6O4, N'-(propan-2-ylidene)pyridine-4-carbohydrazide-1-naphthoic acid (izact-1nta), C9H11N3O·C11H8O2, N'-(butan-2-ylidene)pyridine-4-carbohydrazide-2-chloro-4-nitrobenzoic acid (izbt-2c4n), C10H13N3O·C7H4ClNO4, and N'-(butan-2-ylidene)pyridine-4-carbohydrazide-2,5-dihydroxybenzoic acid (izbt-2,5-dhba), C10H13N3O·C7H6O4. The cocrystals containing izbt were compared to those containing the same (or similar) coformers with izact that have been reported either here or in the Cambridge Structural Database (CSD). Most of the cocrystals showed different packing despite having the same hydrogen-bonding motifs. The cocrystals were characterized by single-crystal X-ray diffraction (SC-XRD), powder X-ray diffraction (PXRD) and differential scanning calorimetry (DSC).

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来源期刊
Acta Crystallographica Section C Structural Chemistry
Acta Crystallographica Section C Structural Chemistry CHEMISTRY, MULTIDISCIPLINARYCRYSTALLOGRAPH-CRYSTALLOGRAPHY
CiteScore
1.60
自引率
12.50%
发文量
148
期刊介绍: Acta Crystallographica Section C: Structural Chemistry is continuing its transition to a journal that publishes exciting science with structural content, in particular, important results relating to the chemical sciences. Section C is the journal of choice for the rapid publication of articles that highlight interesting research facilitated by the determination, calculation or analysis of structures of any type, other than macromolecular structures. Articles that emphasize the science and the outcomes that were enabled by the study are particularly welcomed. Authors are encouraged to include mainstream science in their papers, thereby producing manuscripts that are substantial scientific well-rounded contributions that appeal to a broad community of readers and increase the profile of the authors.
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