Home Cart Sign in  
Chemical Structure| 896114-82-2 Chemical Structure| 896114-82-2

Structure of 896114-82-2

Chemical Structure| 896114-82-2

*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 [ 896114-82-2 ]

CAS No. :896114-82-2
Formula : C12H8N4O2
M.W : 240.22
SMILES Code : O=[N+](C1=CN=C(N=C(C2=CC=CC=C2)N3)C3=C1)[O-]

Safety of [ 896114-82-2 ]

Application In Synthesis of [ 896114-82-2 ]

* 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 [ 896114-82-2 ]

[ 896114-82-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 100-52-7 ]
  • [ 3537-14-2 ]
  • [ 896114-82-2 ]
YieldReaction ConditionsOperation in experiment
In nitrobenzene; at 140 - 150℃; for 15h; Experimental Procedures; Starting materials; 2-phenyl-3H-imidazo[4,5-blpyridin-6-ylamine; a); 6-Nitro-2-phenyl-3H-imidazo[4,5-b] pyridine; 14.05 g <strong>[3537-14-2]2,3-diamino-5-nitropyridine</strong> and 9.68 g benzaldehyde in 250 mL nitrobenzene were heated to 140-150 0C for 15 hours (hrs). The solvent is removed by vacuum distillation and the residue is dispersed in ethyl acetate, filtered, and the filter residue washed thoroughly with ethyl acetate.Yield 16.0 g
In nitrobenzene; at 140 - 150℃; for 15h; Example a) 6-Nitro-2-phenyl-3H-imidazo[4,5-b]pyridine; 14.05 g <strong>[3537-14-2]2,3-diamino-5-nitropyridine</strong> and 9.68 g benzaldehyde in 250 ml nitrobenzene were heated to 140-150 0C for 15 hrs. The solvent is removed by vacuum distillation and the residue is dispersed in ethyl acetate, filtered, and the filter residue washed thoroughly with ethyl acetate. Yield 16.O g
In nitrobenzene; at 140 - 150℃; for 15h; 14.05 g <strong>[3537-14-2]2,3-diamino-5-nitropyridine</strong> and 9.68 g benzaldehyde in 250 ml nitrobenzene were heated to 140-150 C. for 15 hrs. The solvent is removed by vacuum distillation and the residue is dispersed in ethyl acetate, filtered, and the filter residue washed thoroughly with ethyl acetate. Yield 16.0 g
In nitrobenzene; at 140 - 150℃; for 15h; Example 1-1 (2-Phenyl-3H-imidazo[4,5-b]pyridin-6-yl)-carbamic acid 1-methyl-allyl ester a) 6-Nitro-2-phenyl-3H-imidazo[4,5-b]pyridine; 14.05 g <strong>[3537-14-2]2,3-diamino-5-nitropyridine</strong> and 9.68 g benzaldehyde in 250 ml nitrobenzene were heated to 140-150 C. for 15 hrs. The solvent is removed by vacuum distillation and the residue is dispersed in ethyl acetate, filtered, and the filter residue washed thoroughly with ethyl acetate. Yield 16.0 g

  • 2
  • [ 3537-14-2 ]
  • [ 65-85-0 ]
  • [ 896114-82-2 ]
YieldReaction ConditionsOperation in experiment
43% With trichlorophosphate; for 16h;Reflux; 5-Nitropyridine-2,3-diamine (100 mg, 0.65 mmol, see Example 1) and benzoic acid (87 mg, 0.71 mmol, 1.1 eq.) were combined in POCl3 (5 mL) and heated to reflux for 16 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure, and the resulting residue was taken up in saturated sodium bicarbonate solution, and extracted with 25% IPA/DCM (2 X). The extracts were dried over sodium sulfate and concentrated to 6-nitro-2-phenyl-3H-imidazo[4,5-b]pyridine (67 mg, 43%) as a solid. 1H NMR (400 MHz, DMSO-d6) delta 9.24-9.27 (m, IH), 8.81 (br s, IH), 8.27-8.32 (m, 2H), 7.61-7.67 (m, 3H); m/z (APCI-neg) M-I = 239.3.
 

Historical Records

Technical Information

Categories