Home Cart Sign in  
Chemical Structure| 50596-36-6 Chemical Structure| 50596-36-6

Structure of 50596-36-6

Chemical Structure| 50596-36-6

*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 [ 50596-36-6 ]

CAS No. :50596-36-6
Formula : C13H11NO3
M.W : 229.23
SMILES Code : O=C(O)C1=CC=C(OCC2=NC=CC=C2)C=C1
MDL No. :MFCD08098737

Safety of [ 50596-36-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 50596-36-6 ]

* 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 [ 50596-36-6 ]

[ 50596-36-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 50596-36-6 ]
  • [ 22237-12-3 ]
  • [ 1126369-28-5 ]
YieldReaction ConditionsOperation in experiment
92% To 4-(pyridin-2-ylmethoxy)benzoic acid (300 mg, 1.31 mmol), HATU (522 mg, 1.37 mmol) and DIPEA (0.457 mL, 2.62 mmol) was added DMF (3 mL). After stirring for 1 h at 50 0C, the mixture was cooled and 3-amino-4-methylphenylboronic acid (198 mg, 1.31 mmol) was added. The reaction was reheated to 50 0C for 6 h , an additional equivalent of 3- amino-4-methylphenylboronic acid was added, and the reaction was stirred at RT for 48h. The reaction was poured into sat. NaCl solution (30 mL). The precipitate was filtered, washed with water, followed by Et2O, and dried under suction to yield the title compound (434 mg, 92 %). 1R NMR (DMSO-de) δ 9.75 (s, IH), 8.61 (d, IH), 7.96 (d, 2H), 7.90 (td, IH), 7.67 (s, IH), 7.58 (m, 2H), 7.40 (dd, IH), 7.22 (d, IH), 7.14 (d, 2H), 5.29 (s, 2H), 2.20 (s, 3H). MS (M+H+) = 363.
92% With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 - 50℃; for 65h; To 4-(pyridin-2-ylmethoxy)benzoic acid (300 mg, 1.31 mmol), HATU (522 mg, 1.37 mmol) and DIPEA (0.457 mL, 2.62 mmol) was added DMF (3 mL). After stirring for 1 h at 50 C, the mixture was cooled and 3-amino-4-methylphenylboronic acid (198 mg, 1.31 mmol) was added. The reaction was reheated to 50 C for 6 h. As HOAt ester was still present, an additional equivalent of 3-amino-4-methylphenylboronic acid was added, and the reaction was stirred at RT for 48h. The reaction was poured into sat. NaCl solution (30 mL). The precipitate was filtered, washed with water, followed by Et2O, and dried under suction to yield the title compound (434 mg, 92 %). 1H NMR (DMSO-d6) δ ppm 9.75 (s, 1H), 8.61 (d, 1H), 7.96 (d, 2H), 7.90 (td, 1H), 7.67 (s, 1H), 7.58 (m, 2H), 7.40 (dd, 1H), 7.22 (d, 1H), 7.14 (d, 2H), 5.29 (s, 2H), 2.20 (s, 3H). LCMS (M+H) = 363.
 

Historical Records