Production Method 1

4175-77-3

4175-78-4

848501-94-0

2136639-03-5

Reaction Conditions

1.1 Reagents: Dimethylacetamide Solvents: Water ;  6 h, 135 - 140 °C

Reference

A facile approach to transformation of hetero aryl amides from hetero aryl halides

Nagaraju, B.; Subbaiah, T.; Prasanna, B., Heterocyclic Letters, 2017, 7(2), 467-472

2-bromo-1,3-thiazole-4-carboxamide Raw materials

• 2,4-Dibromothiazole
• 2,5-Dibromothiazole

2-bromo-1,3-thiazole-4-carboxamide Preparation Products

• 4-Cyano-2-thiazolecarboxamide (2136639-03-5)
• 2-bromo-1,3-thiazole-4-carboxamide (848501-94-0)

• 1. Exceptionally high temperature spin crossover in amide-functionalised 2,6-bis(pyrazol-1-yl)pyridine iron(ii) complex revealed by variable temperature Raman spectroscopy and single crystal X-ray diffraction?
  Max Attwood,Hiroki Akutsu,Lee Martin,Toby J. Blundell,Pierre Le Maguere,Scott S. Turner Dalton Trans., 2021,50, 11843-11851
• 2. Enantiomeric helical TiO2 nanofibers modulate different peptide assemblies and subsequent cellular behaviors?
  Xu Jie,Deng Xu,Weili Wei RSC Adv., 2019,9, 29149-29153
• 3. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
  Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
• 4. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
  J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
• 5. Excited state dynamics of symmetric and asymmetric Cr3(dpa)4Cl2 measured using femtosecond transient absorption spectroscopy?
  Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Thiazolecarboxylic acids and derivatives
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Thiazoles Thiazolecarboxylic acids and derivatives

• 933692-77-4(1-(2-Bromothiazol-4-yl)-N-methylmethanamine)
• 1092942-42-1(2-Bromo-N-methyl-1,3-thiazole-4-carboxamide)
• 919784-50-2(Methanone, 1-azetidinyl(2-bromo-4-thiazolyl)-)
• 5198-80-1(2-Bromothiazole-4-carbaldehyde)
• 135298-45-2(2-Bromo-N-cyclopropylthiazole-4-carboxamide)
• 1025468-14-7(2-Bromo-5-methylthiazole-4-carboxamide)
• 1254694-56-8(2-Bromo-5-methylthiazole-4-carboxamide)
• 867333-36-6(2-Bromo-N-(2-(pyrrolidin-1-yl)-ethyl)thiazole-4-carboxamide)
• 933749-24-7((2-Bromothiazol-4-yl)methanamine)
• 478366-00-6(4-THIAZOLECARBONYL AZIDE, 2-BROMO-)