Home Cart Sign in  
Chemical Structure| 133676-16-1 Chemical Structure| 133676-16-1

Structure of 133676-16-1

Chemical Structure| 133676-16-1

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 133676-16-1 ]

CAS No. :133676-16-1
Formula : C18H15NO4
M.W : 309.32
SMILES Code : O=C(C1=CC(C2=CC=C(OC)C(OC)=C2)=NC3=CC=CC=C13)O
MDL No. :MFCD00219544
InChI Key :XJSXKUVHNQWOPH-UHFFFAOYSA-N
Pubchem ID :673703

Safety of [ 133676-16-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 133676-16-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 133676-16-1 ]

[ 133676-16-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 133676-16-1 ]
  • [ 1597-32-6 ]
  • [ 1208372-60-4 ]
YieldReaction ConditionsOperation in experiment
~ 11% With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In dichloromethane; at 20℃;Cooling with ice; To a stirred and ice-cooled solution of 2-(3,4-dimethoxy-phenyl)- quinoline-4-carboxylic acid (INT-3; 2.000 g, 6.4658 mmol) and 6-fluoro-pyridin-2- ylamine (0.870 g, 7.759 mmol) in dichloromethane (20 ml), triethylamine (4.580 g,-15.4 ml, 45.2606 mmol) is added, followed by portion-wise addition of 1 - propanephosphonic acid cyclic anhydride (16.458 g, 25.8632 mmol) and the mixture is allowed to attain room temperature spontaneously overnight and stirred at this temperature for additional 20 hours. The resulting mixture is diluted with dichloromethane (-50 ml), washed with water and brine, dried (MgSO4), and evaporated to afford a brown gummy residue (2.600 g, 100% mass balance). This is purified by column chromatography eluting with 32-36% ethyl acetate in hexane, to obtain the title compound as a pale yellow solid (0.300 g, -11 % yield). M. p. 225.2-226.4C.
~ 11% With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In dichloromethane; at 20℃;Cooling with ice; To a stirred and ice-cooled solution of 2-(3,4-dimethoxy-phenyl)-quinoline-4-carboxylic acid (INT-3; 2.000 g, 6.4658 mmol) and <strong>[1597-32-6]6-fluoro-pyridin-2-ylamine</strong> (0.870 g, 7.759 mmol) in dichloromethane (20 ml), triethylamine (4.580 g, 15.4 ml, 45.2606 mmol) is added, followed by portion-wise addition of 1-propanephosphonic acid cyclic anhydride (16.458 g, 25.8632 mmol) and the mixture is allowed to attain room temperature spontaneously overnight and stirred at this temperature for additional 20 hours. The resulting mixture is diluted with dichloromethane (50 ml), washed with water and brine, dried (MgSO4), and evaporated to afford a brown gummy residue (2.600 g, 100% mass balance). This is purified by column chromatography eluting with 32-36% ethyl acetate in hexane, to obtain the title compound as a pale yellow solid (0.300 g, 11% yield). M.p. 225.2-226.4 C.
 

Historical Records

Technical Information

Categories