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Chemical Structure| 89808-77-5 Chemical Structure| 89808-77-5

Structure of 89808-77-5

Chemical Structure| 89808-77-5

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Product Details of [ 89808-77-5 ]

CAS No. :89808-77-5
Formula : C9H6N2O3
M.W : 190.16
SMILES Code : O=[N+](C1=CC(C2=CN=CO2)=CC=C1)[O-]
MDL No. :MFCD00085147

Safety of [ 89808-77-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H319
Precautionary Statements:P301+P310-P305+P351+P338
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 89808-77-5 ]

* 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 [ 89808-77-5 ]

[ 89808-77-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 89808-77-5 ]
  • [ 157837-31-5 ]
YieldReaction ConditionsOperation in experiment
93% With hydrogenchloride; tin(II) chloride dihdyrate; water; In ethanol; at 20℃; A solution of intermediate la (3.52g, 18.5mmol) in absolute ethanol (210ml) was treated with water (21ml) then SnCI2.2H20 (20.9g, 92.6mmol) and cone. HCI (15ml, 180mmol). After stirring at room temperature overnight, the solution was taken to pH 7 with 10% aqueous NaOH solution and extracted repeatedly with EtOAc. The organics were dried (MgS04), filtered and evaporated to afford the title compound as a pale orange powder (2.74g, 93%). *H NMR (400 MHz, DMSO-d6) δ 8.37 (s, 1H), 7.49 (s, 1H), 7.10 (t, J = 7.8 Hz, 1H), 6.90 (t, J = 1.8 Hz, 1H), 6.86 (d, J = 7.6 Hz, 1H), 6.59 - 6.54 (m, 1H), 5.25 (s, 2H).
93% With hydrogenchloride; tin(II) chloride dihdyrate; In ethanol; water; at 20℃; [0087] A solution of intermediate Ia (3.52g, 18.5mmol) in absolute ethanol (210ml) was treated with water (21ml) thenSnCl2.2H2O (20.9g, 92.6mmol) and conc. HCl (15ml, 180mmol). After stirring at room temperature overnight, the solutionwas taken to pH 8 with 10% aqueous NaOH solution and extracted repeatedly with EtOAc. The organics were dried(MgSO4), filtered and evaporated to afford the title compound as a pale orange powder (2.74g, 93%). 1H NMR (400MHz, DMSO-d6) δ 8.37 (s, 1H), 7.49 (s, 1H), 7.10 (t, J = 7.8 Hz, 1H), 6.90 (t, J = 1.8 Hz, 1H), 6.86 (d, J = 7.6 Hz, 1H),6.59 - 6.54 (m, 1H), 5.25 (s, 2H).
83% 1 g (5.26 mmol, 1 eq.) of 5-(3-nitrophenyl)oxazole and 10 mL of TFA are introduced into a 1 L flask. 1 g of zinc is carefully added in a plurality of batches. The mixture is stirred for 2 hours at room temperature then is poured over ice. Sodium hydroxide is slowly added <n="56"/>until the medium becomes basic, and the medium is extracted with diethyl ether. The organic phase is washed with a 1 M solution of HCl and the impurities are extracted with diethyl ether. The aqueous phase is again basified with sodium hydroxide and the product is extracted with diethyl ether. The organic phases are combined, dried over MgSO4 and filtered. After concentration to dryness, 700 mg (yield = 83 %) of aniline 3-oxazol-5-yl- phenylamine are obtained, in the form of a beige solid. The product is used without subsequent purification.1H NMR(400 MHz, CD3OD): ppm 6.74 (d, IH, aromatic H), 7.05 (d, IH, aromatic H), 7.09 (s, IH, aromatic H), 7.18 (t, IH, aromatic H), 7.41 (s, IH, Hoxazoie), 8.22 (s, IH, Hoxazoie). MS: 16I+ (M+H)+
With hydrogen;5% palladium over charcoal; In ethanol; ethyl acetate; at 20℃; for 15h; Reference Example 9 3-(Oxazol-5-yl)phenylamine 3-(Oxazol-5-yl)nitrobenzene (3.56 g) was dissolved in ethanol (80 ml) and ethyl acetate (80 ml), 5% palladium-carbon (1.9 g) was added to the mixture and stirred at room temperature for 15 hours in an atmosphere of hydrogen. After filtration of the catalyst, the solvent was evaporated, and the thus obtained crystals were washed with hexane to obtain the title compound (2.80 g) as a white solid. 1H-NMR (400 MHz, CDCl3) δ: 3.77 (2H, br s), 6.66 (1H, d, J=7.8 Hz), 6.98 (1H, br s), 7.05 (1H, br d, J=7.9 Hz), 7.20 (1H, t, J=8.1 Hz), 7.30 (1H, s), 7.88 (1H, s). FAB-MS m/z: 161 (M+H)+.

 

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