Home Cart Sign in  
Chemical Structure| 959617-73-3 Chemical Structure| 959617-73-3

Structure of 959617-73-3

Chemical Structure| 959617-73-3

*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 [ 959617-73-3 ]

CAS No. :959617-73-3
Formula : C13H15N3O2
M.W : 245.28
SMILES Code : O=C(OC(C)(C)C)NC1=CC2=NC=CC=C2N=C1
MDL No. :MFCD24467536

Safety of [ 959617-73-3 ]

Application In Synthesis of [ 959617-73-3 ]

* 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 [ 959617-73-3 ]

[ 959617-73-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 959617-73-3 ]
  • [ 14756-77-5 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; water; In methanol; at 50℃; for 2h; To a solution of tert-butyl l,5-naphthyridin-3-ylcarbamate (D-12) (4.040 g, 16.5 mmol, 1.0 eq) in methanol (24 mL), concentrated hydrochloric acid (36.5%, 10 mL, 120 mmol, 7.27 eq) was added. The resulting mixture was stirred at 50 C for 2 h. The reaction was complete based on TLC analysis. The mixture was concentrated under reduced pressure to afford the desired product l,5-naphthyridin-3-amine (D-13), which was used for next reaction without further purification. 'HNMR (300 MHz, DMSO-<¾) 8.85 (m, 1H), 8.77-8.75 (m, 2H),7.63-7.69(m, 1H), 7.4 (d, J= 1.8 Hz, 1H); ESI-MS m/z : 146.10 [M+H]+.
With hydrogenchloride; In methanol; water; at 50℃; for 2h; Example 2b: Synthesis of l,5-naphthyridin-3-amine [00316] To a solution of tert-butyl l,5-naphthyridin-3-ylcarbamate (D-12) (4.040 g, 16.5 mmol, 1.0 eq) in methanol (24 mL), concentrated hydrochloric acid (36.5%, 10 mL, 120 mmol, 7.27 eq) was added. The resulting mixture was stirred at 50 C for 2 h. The reaction was complete based on TLC analysis. The mixture was concentrated under reduced pressure to afford the desired product 1 ,5- naphthyridin-3 -amine (D-13), which was used for next reaction without further purification. 'HNMR (300 MHz, DMSO- 6) 8.85 (m, 1H), 8.77-8.75 (m, 2H),7.63-7.69(m, 1H), 7.4 (d, J = 1.8 Hz, 1H); ESI-MS m/z : 146.10 [M+H]+.
To a solution of 1.00 g of tert-butyl 1,5-naphthyridin-3-ylcarbamate in 6 mL of methanol, 1 mL of a 12 mol/L aqueous hydrogen chloride solution was added, and the mixture was stirred for 30 minutes. To the reaction mixture, 5 mL of methanol and 1 mL of a 12 mol/L aqueous hydrogen chloride solution were added, and the mixture was stirred at 40C for 40 minutes, and at 80C for 40 minutes. In the reaction mixture, the solvent was distilled off under reduced pressure, the mixture was neutralized with a saturated aqueous sodium hydrogen carbonate solution, and then the solvent was distilled off under reduced pressure. The resultant residue was washed with ethanol and, in the mother liquid, the solvent was distilled off under reduced pressure, and the resultant residue was purified with silica gel column chromatography using silica gel; Chromatorex-NH made by Fuji Silysia Chemical Ltd., and an eluent of chloroform:methanol = 10:1 to obtain 0.50 g of 1,5-naphthyridin-3-amine as a yellow solid. 1H-NMR (CDCl3) δ: 4.18 (2H, s), 7.31-7.42 (1H, m), 7.43-7.50 (1H, m), 8.21-8.30 (1H, m), 8.51-8.62 (1H, m), 8.77-8.88 (1H, m)
 

Historical Records

Technical Information

Categories