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Chemical Structure| 55687-29-1 Chemical Structure| 55687-29-1

Structure of 55687-29-1

Chemical Structure| 55687-29-1

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Product Details of [ 55687-29-1 ]

CAS No. :55687-29-1
Formula : C9H10N2O2
M.W : 178.19
SMILES Code : COC1=CC=C2NCC(=O)NC2=C1
MDL No. :MFCD13659372

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Application In Synthesis of [ 55687-29-1 ]

* 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 [ 55687-29-1 ]

[ 55687-29-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 55687-29-1 ]
  • [ 55687-30-4 ]
YieldReaction ConditionsOperation in experiment
To a solution of 8% aqueous sodium hydroxide (1.32 L) was added 7-methoxy-3,4- dihydroquinoxalin-2(lH)-one (Intermediate 16, 100 g) followed by a solution of 3 wt% hydrogen peroxide in water (1.17 L). The reaction mixture was slowly heated to 80 0C and maintained at this temperature for 4 hours. Then the heating source was removed and acetic acid (150 mL) was added dropwise. The suspension was stirred overnight at room temperature and the precipitated solid was collected by filtration to afford the product as a tan solid (90 g).MS (ESP): 177 (MH+) for C9H8N2O21H-NMR (DMSO-d*) δ: 3.83 (s, 3H); 6.76 (d, IH); 6.90 (dd, IH); 7.67 (d, IH); 7.97 (s,IH); 12.32 (brs, IH).
To a solution of 8% aqueous sodium hydroxide (1.32 L) was added 7-methoxy-3,4- dihydroquinoxalin-2(lH)-one (Intermediate 8, 100 g), followed by a solution of 3 wt% hydrogen peroxide in water (1.17 L). The reaction mixture was slowly heated to 80 0C and maintained at this temperature for 4 hours. The heating source was then removed and acetic acid (150 mL) was added dropwise. The suspension was stirred overnight at room temperature and the precipitated solid was collected by filtration to afford the product as a tan solid (90 g).MS (ES): 177 (MH+) for C9H8N2O21H NMR (DMSO-d.) δ: 3.83 (s, 3H); 6.76 (d, IH); 6.90 (dd, IH); 7.67 (d, IH); 7.97 (s,IH); 12.32 (brs, IH)
2 g To a stirred solution of Compound 26b (3g,16.85mmol) in 8%NaOH solution(39.6ml) was added 30%H2O2 solution(35.1ml) at RT. The reaction was heated at 80C for 4h afterwhich was added AcOH (4.5ml) dropwise at RT. Upon completion, the filtered solids were given water and diethyl ether washings to afford the required compound (2g) as an off-white solid.
Intermediate 237-Methoxyquinoxalin-2(lH)-oneTo a solution of 8% aqueous sodium hydroxide (1.32 L) was added 7-methoxy-3,4- dihydroquinoxalin-2(lH)-one (Intermediate 22) (100 g) followed by a solution of 3 wt% hydrogen peroxide in water (1.17 L). The reaction mixture was slowly heated to 80 0C and maintained at this temperature for 4 hours. Then the heating source was removed and acetic acid (150 mL) was added dropwise. The suspension was stirred overnight at room temperature and the precipitated solid was collected by filtration to afford the product as a tan solid (90 g).MS (ESV. 177 (MH+) for C9H8N2O21H-NMR (DMSO-dfi) δ: 3.83 (s, 3H); 6.76 (d, IH); 6.90 (dd, IH); 7.67 (d, IH); 7.97 (s,IH); 12.32 (brs, IH).
208 mg To a solution of 8% aqueous sodium hydroxide (4.5 mL) was added 3 (340 mg) followed by a solution of 30 wt % hydrogen peroxide in water (1.97 mL). The reaction mixture was slowly heated to 80 C and maintained at this temperature for 4 ii. The mixturewas cooled down to room temperature, and acetic acid (510 iL) was added dropwise. The suspension was stirred overnight at room temperature and the precipitated solid was collected by filtration to afford 4 as a tan solid (208 mg, 51% for two steps). ‘H NMR (DMSO-d6) : 3.83 (s, 3H); 676 (d, IH); 6.89-6.93 (dd, IH); 7.67-7.70 (d, IH); 7.97 (s, 1EI); 12.30 (hrs, 1Ff). (See Reck. F.; et al., J. Med. Chem. 2011, 54. 7834.)

 

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