2-Aminothiazole
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| Appearance | Light yellow crystals |
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| Template:Longitem | −56.0·10−6 cm3/mol |
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2-Aminothiazole is a heterocyclic amine featuring a thiazole core. It can also be considered a cyclic isothiourea. It possesses an odor similar to pyridine and is soluble in water, alcohols and diethyl ether. 2-Aminothiazole itself is mainly of academic interest, with few exceptions. It is a precursor to a sulfathiazole ("sulfa drugs"). 2-Aminothiazole can be used as a thyroid inhibitor in the treatment of hyperthyroidism.[1]
2-Aminothiazole is prepared from paraldehyde, thiourea, and sulfuryl chloride.[2]
2-Aminothiazoles
Like the parent, 2-aminothiazoles are often produced by the condensation of thiourea and an alpha-halo ketone.[3][4][5]
Hantsch Thiazole Synthesis Hantsch Thiazole Synthesis
In an adaptation of the Robinson-Gabriel synthesis, a 2-acylamino-ketone reacts with phosphorus pentasulfide.
Applications
Synthetic aminothiazoles - compounds containing the parent 2-aminothiazole as a subunit - are used in medicinal chemistry. Some examples are abafungin, acotiamide, amiphenazole, amthamine, avatrombopag, aztreonam, cefepime, cefixime, ceftizoxime, ceftiofur, ceftibuten, cefpirome, famotidine, meloxicam, and pramipexole.[6][7]
References
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