Home Cart Sign in  
Chemical Structure| 1174046-76-4 Chemical Structure| 1174046-76-4

Structure of 1174046-76-4

Chemical Structure| 1174046-76-4

*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 [ 1174046-76-4 ]

CAS No. :1174046-76-4
Formula : C24H17ClFN3O
M.W : 417.86
SMILES Code : ClC1=C(OC2=CC=C(N)C=C2F)C=CN=C1N=C(C3=CC=CC=C3)C4=CC=CC=C4
MDL No. :N/A

Safety of [ 1174046-76-4 ]

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

Application In Synthesis of [ 1174046-76-4 ]

* 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 [ 1174046-76-4 ]

[ 1174046-76-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1052114-81-4 ]
  • [ 1174046-76-4 ]
  • [ 1174047-03-0 ]
YieldReaction ConditionsOperation in experiment
78% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20℃; for 3h; To a solution of 4-(4-amino-2-fluorophenoxy)-3-chloro-N- (diphenylmethylene)pyridin-2-amine (836 mg, 2.0 mmol) and 5-(4-fluorophenyl)-4- <n="39"/>oxo-l^-dihydropyridine-S-carboxylic acid (490 mg, 2.0 mmol) in DMF (10 mL) at room temperature were added HATU (913 mg, 2.4 mmol) and DIPEA (1.05 ml, 6.0 mmol). The reaction mixture was stirred at room temperature for 3 h prior to being quenched by the addition of cold water (50 mL). The solid that formed was collected by filtration, and washed with water and ether. The solid was dissolved in DCM and purified by flash column chromatography (SiC^, DCM to 10% MeOH in DCM) to give the desired product (987 mg, 78%) as a light yellow solid. MS(ESI+) m/z 633 (M + H)+.
 

Historical Records

Technical Information

Categories