Home Cart Sign in  
Chemical Structure| 72569-97-2 Chemical Structure| 72569-97-2

Structure of 72569-97-2

Chemical Structure| 72569-97-2

*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 [ 72569-97-2 ]

CAS No. :72569-97-2
Formula : C7H11NO3
M.W : 157.17
SMILES Code : C/C(NC(C)=O)=C\C(OC)=O
MDL No. :N/A

Safety of [ 72569-97-2 ]

Application In Synthesis of [ 72569-97-2 ]

* 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 [ 72569-97-2 ]

[ 72569-97-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52023-68-4 ]
  • [ 72569-97-2 ]
  • [ 1542257-81-7 ]
YieldReaction ConditionsOperation in experiment
39% To a solution of 6-morpholinopyridin-3 -amine (1.79 g, 10 mmol) in CH2C12(100 mL) was added trimethylaluminium (40 mL, 40 mmol, 1 M in heptane) carefully under N2. The mixture was stirred at rt for 30 min, followed by the addition of a solution of methyl 3-acetaminocrotonate (1.89 g, 12 mmol) in CH2C12(5 mL). The reaction was stirred at rt for 6 h, then quenched with saturated NH4C1 aqueous solution (100 mL). The organic phase was dried over anhydrous Na2S04and concentrated in vacuo. The residue was purified by recrystallized from EtOAc to give the title compound as a pale yellow solid (1.11 g, 39%). The compound was characterized by the following spectroscopic data:MS (ESI, pos.ion) m/z: 287.2 (M+l); 1H-NMR (400 MHz, CDCl3): 2.22 (s, 3 H), 2.30 (s, 3 H), 3.54-3.60 (m, 4 H), 3.83 (t, 4 H, J = 4.9 Hz), 6.29 (s, 1 H), 6.74 (d, 1 H, J = 8.8 Hz), 7.33 (dd, 1 H, J, = 2.1 Hz, J2= 8.8 Hz), 8.00 (d, 1 H, J = 2.6 Hz).
39% To a solution of 6-morpholinopyridin-3-amine (1.79 g, 10 mmol) in CH2Cl2 (100 mL) was added trimethylaluminium (40 mL, 40 mmol, 1 M in heptane) carefully under N2. The mixture was stirred at rt for 30 min, followed by the addition of a solution of methyl 3-acetaminocrotonate (1.89 g, 12 mmol) in CH2Cl2 (5 mL). The reaction was stirred at rt for 6 h, then quenched with saturated NH4Cl aqueous solution (100 mL). The organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by recrystallized from EtOAc to give the title compound as a pale yellow solid (1.11 g, 39%). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 287.2 (M+1); 1H-NMR (400 MHz, CDCl3): delta 2.22 (s, 3H), 2.30 (s, 3H), 3.54-3.60 (m, 4H), 3.83 (t, 4H, J=4.9 Hz), 6.29 (s, 1H), 6.74 (d, 1H, J=8.8 Hz), 7.33 (dd, 1H, J1=2.1 Hz, J2=8.8 Hz), 8.00 (d, 1H, J=2.6 Hz).
 

Historical Records