Home Cart Sign in  
Chemical Structure| 1223003-51-7 Chemical Structure| 1223003-51-7

Structure of 1223003-51-7

Chemical Structure| 1223003-51-7

*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 [ 1223003-51-7 ]

CAS No. :1223003-51-7
Formula : C14H18F3N3O
M.W : 301.31
SMILES Code : CCC(N1CCN(C2=CC=C(N)C=C2C(F)(F)F)CC1)=O
MDL No. :N/A

Safety of [ 1223003-51-7 ]

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

Application In Synthesis of [ 1223003-51-7 ]

* 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 [ 1223003-51-7 ]

[ 1223003-51-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1223003-51-7 ]
  • [ 21168-41-2 ]
  • [ 1223003-25-5 ]
YieldReaction ConditionsOperation in experiment
93% In 1,4-dioxane; at 20 - 80℃; To a solution of 5.0 <strong>[21168-41-2]ethyl 4,6-dichloroquinoline-3-carboxylate</strong> (1.08 g, 4 mmol, 1 equiv.) in 1,4-dioxane (10 mL) at room temperature was added compound 5.1 l-(4- (4-amino-2-(trifluoromethyl)phenyl)piperazin-1-yl)propan-1-one (1.2 g, 4 mmol, 1 equiv.). The resulting solution was heated to 8OC and stirred 4h before cooling to room temperature. NaOH (IN aqueous solution, 3 mL) was added. The solution was diluted with EtOAc (30 mL) and washed with water (30 mL X2) and brine (30 mL). The organic phase was dried over Na2SO4. After removal of solvents, the residue was purified via flash chromatography (CH2Cl2: MeOH =20:1) to afford the desired product 5.2 ethyl 6-chloro-4-(4-(4- propionylpiperazin-1-yl)-3-(trifluoromethyl)phenylamino)quinoline-3-carboxylate (2g; 93%). LC-MS: (M+H) : 622.20
 

Historical Records