374784-55-1

Basic information

• Product Name: tert-butyl [6-{3-[(tert-butoxycarbonyl)amino]-5-nitrophenyl}-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetate
• Synonyms: tert-butyl [6-{3-[(tert-butoxycarbonyl)amino]-5-nitrophenyl}-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetate
• CAS NO: 374784-55-1
• Molecular Weight: 502.568
• Mol File: 374784-55-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl [6-{3-[(tert-butoxycarbonyl)amino]-5-nitrophenyl}-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl [6-{3-[(tert-butoxycarbonyl)amino]-5-nitrophenyl}-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetate(374784-55-1)
• EPA Substance Registry System: tert-butyl [6-{3-[(tert-butoxycarbonyl)amino]-5-nitrophenyl}-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetate(374784-55-1)

Safety Data

• Hazardous Substances Data: 374784-55-1(Hazardous Substances Data)

Upstream product

• 626-05-1 2,6-Dibromopyridine 
• 374784-53-9 6-bromo-3-(isopropylamino)pyridin-2-ol 
• 374784-52-8 6-bromo-N-isopropyl-2-methoxypyridin-3-amine 
• 89466-18-2 6-bromo-2-methoxy-pyridin-3-ylamine 
• 39856-57-0 2,6-dibromo-3-aminopyridine 
• 374784-54-0 tert-butyl [6-bromo-3-(isopropylamino)-2-oxo-pyridin-1(2H)-yl]acetate 
• 55304-80-8 2,6-dibromo-3-nitropyridine 

Downstream Products

• 618398-72-4 benzyl (1E)-amino{4-[({[6-(3-amino-5-nitrophenyl)-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetyl}amino)methyl]phenyl}methylidenecarbamate 
• 618398-72-4 benzyl (1E)-amino{4-[({[6-(3-amino-5-nitrophenyl)-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetyl}amino)methyl]phenyl}methylenecarbamate 
• 618398-61-1 [6-(3-amino-5-nitrophenyl)-3-(isopropylamino)-2-oxopyridin-1(2H)-yl]acetic acid 

Relevant articles and documents

Design, Synthesis, and Crystal Structure of Selective 2-Pyridone Tissue Factor VIIa Inhibitors

Targeted 2-pyridones were selected as tissue Factor VIIa inhibitors and prepared from 2,6-dibromopyridine via a multistep synthesis. A variety of chemical transformations, including regioselective nucleophilic addition, selective nitrogen alkylation, and