72100-53-9

Upstream product

• 420-04-2 CYANAMID 
• 72100-41-5 2-Morpholinyl-5-phenyl-1,3-oxathiolium 
• 110-91-8 morpholine 
• 39736-27-1 [4-amino-2-(methylthio)thiazole-5-yl](phenyl)methanone 
• 13145-41-0 potassium cyanocarbonimidodithioate 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 72100-74-4 N-(5-Benzoyl-2-morpholin-4-yl-thiazol-4-yl)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetamide 
• 1443014-95-6 (4-bromo-2-morpholino-1,3-thiazol-5-yl)(phenyl)methanone 
• 1443014-94-5 (4-chloro-2-morpholino-1,3-thiazol-5-yl)(phenyl)methanone 
• 72100-85-7 4-<(Aminoacetyl)amino>-5-benzoyl-2-morpholinothiazole hydrobromide 
• 72100-99-3 5-Acethydrazino-2-morpholino-8-phenyl-6H-thiazolo<4,5-e><1,4>diazepine 
• 72101-00-9 1-Methyl-8-morpholino-6-phenyl-4H-s-triazolo<3,4-c>thiazolo<4,5-e><1,4>diazepine 
• 72100-90-4 4,6-Dihydro-8-phenyl-2-morpholinothiazolo<4,5-e><1,4>diazepin-5(5H)-one 
• 72100-76-6 5-Benzoyl-4-<<((benzoxycarbonyl)amino)acetyl>amino>-2-morpholinothiazole 

Relevant academic research and scientific papers

Heterocondensed thiophenes and thiazoles by Thorpe-Ziegler cyclization

(Chemical Equation Presented) The syntheses of novel thieno-pyridones, thiazolo-pyridones, thiazolo-pyridines and amino- and diamino-dieno-pyridines were described. Simultaneously, it was demonstrated that in these compounds and in the related 3-aminothio

Traceless solid-phase synthesis of 2,4,5-trisubstituted thiazoles

The solid-phase synthesis of trisubstituted thiazoles is described. The synthetic strategy involves the formation of a polymer-bound thiazole by reacting resin-bound cyanodithioimidocarbonic acid and α-bromoketone. The resin-bound thiazole was reacted with acyl chlorides or isocyanates. After oxidation-activation of a thioether linker to a sulfone linker, traceless cleavage was achieved with nucleophiles to give trisubstituted thiazoles. Georg Thieme Verlag Stuttgart.

Heterocyclic Cation Systems. 14. Synthesis of Thienodiazepine, Thiazolodiazepine, and s-Triazolothiazolodiazepine Derivatives

Synthesis of heterodiazepines is described.The synthetic route involved reactions of the anion of malononitrile or cyanamide toward 2-substituted 1,3-oxathiolium cation 1 to give amino ketone derivatives 3 and 4 as the key intermediates.Introducti