Synthetic Route of 6118-51-0, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 6118-51-0, Name is exo-3,6-Epoxy-1,2,3,6-tetrahydrophthalic Anhydride, SMILES is O=C1OC([C@@]2([H])[C@](O3)([H])C=C[C@]3([H])[C@]21[H])=O, belongs to thiazolidines compound. In a article, author is Heydari, Reza, introduce new discover of the category.
Synthesis and Crystal Structures of Some Pyridyl Aminothiazole and Thiazolidin-2-ylidene Benzamide Derivatives
Background: Thiazoles and their derivatives are attracting continuing interest over the years because of their varied biological activities. Thiazole and in particular the 2-amino thiazole moiety has been incorporated into a wide variety of therapeutically interesting candidates including antibacterial, anti-HIV, hypertension, anti-inflamenmatory, anti-viral and anticancer agents. Methods: Several methods for the synthesis of thiazole derivatives have been developed. The most widely used method being the Hantzch’s synthesis. In this paper, we describe an efficient one-pot method for the synthesis of some thiazolidin-2-ylidene benzamide and aminothiazole derivatives via condensation of 3-aminopyridine or 2-aminopyridine with phenacyl bromide and benzoyl isothiocyanates. Results: The reaction of 3-aminopyridine, benzoyl isothiocyanates, and phenacyl bromide in the presence of triethylamine yields thiazolidin-2-ylidene benzamides, which upon heating in acetic acid produce pyridyl aminothiazole derivatives. Also the pyridyl aminothiazole derivatives were obtained by the reaction of 2-aminopyridine with benzoyl isothiocyanates and phenacyl bromide in the presence of triethylamine. The molecular structures of the 4-chloro-N-(4-hydroxy-4-phenyl-3-(pyridin-3-yl)thiazolidin-2-ylidene)benzamide, phenyl(4-phenyl-2-(pyridin-3-ylamino)thiazol-5-yl)methanone and (4-phenyl-2-(pyridin-2-yl amino)thiazol-5-yl)(o-tolyl)methanone, have been fully determined by means of single crystal Xray diffraction methods. Conclusion: In summary, present study reports one-pot synthesis of thiazolidin-2-ylidene substituted benzamide and pyridyl aminothiazole derivatives via condensation of 3-aminopyridine or 2-aminopyridine with phenacyl bromide and substituted benzoyl isothiocyanates. The single crystal X-Ray diffraction analysis reveals unequivocally the exact identity of the compounds.
Synthetic Route of 6118-51-0, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 6118-51-0.
Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com