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Chemical Structure| 304902-95-2 Chemical Structure| 304902-95-2

Structure of 304902-95-2

Chemical Structure| 304902-95-2

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Product Details of [ 304902-95-2 ]

CAS No. :304902-95-2
Formula : C8H7BrN2O2
M.W : 243.06
SMILES Code : O=C(C1=NC(C2CC2)=NC=C1Br)O
MDL No. :MFCD11870587

Safety of [ 304902-95-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 304902-95-2 ]

* 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 [ 304902-95-2 ]

[ 304902-95-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 766-38-1 ]
  • [ 57297-29-7 ]
  • [ 304902-95-2 ]
YieldReaction ConditionsOperation in experiment
72% NaH (60percent purity, 41 .9 g,) is added in portions to EtOH (800 mL) at 0 °C. The resulting mixture is warmed to ambient temperature and the cyclopropanecarboxamidine hydrochlorid (93.5 g,) isadded in portions. The reaction is warmed to 50 °C and maintained at this temperature for 0.5 h and then cooled to ambient temperature before mucobromic acid (100 g,) is added in EtOH while keeping the internal temperature below 55 °C. The mixture is allowed to cool to ambient temperature and stirred for additional 16 h. All solid components are removed by filtration and the resulting solution is concentrated under reduced pressure. Aq. HCI (1 mol/L) is added, the aqueous phase is washed with EtOAc (3x), the combined organic extracts are dried over MgSO4 and the solid parts removed by filtration. The residue is concentrated under reduced pressure and the resulting solid titrated with (iPr)20. The solids are collected by filtration and dried yielding the title compound (68.0 g, yield 72 percent) as a colorless solid.1 NMR (400 MHz, CDCI3): 6 = 8.91 (s, 1H), 2.38?2.26 (m, 1H), 1.34?1.14 (m, 4H) ppm; MS (ESI) mlz 244.9 [M + Hj.
72% NaH (60percent purity, 41 .9 g) is added in portions to EtOH (800 mL) at 0 °C. The resulting mixture is warmed to ambient temperature and the cyclopropanecarboxamidine hydrochlorid (93.5 g,) is added in portions. The reaction is warmed to 50 °C and maintained at this temperature for 0.5 hand then cooled to ambient temperature before mucobromic acid (100 g) is added in EtOH while keeping the internal temperature below 55 °C. The mixture is allowed to cool to ambient temperature and stirred for additional 16 h. All solid components are removed by filtration and the resulting solution is concentrated under reduced pressure. Aq. HCI (1 mol/L) is added, the aqueous phase is washed with EtOAc (3x), the combined organic extracts are dried overMg504 and the solid parts removed by filtration. The residue is concentrated under reduced pressure and the resulting solid titrated with (iPr)20. The solids are collected by filtration and dried yielding the title compound (68.0 g, yield 72 percent) as a colorless solid.1H NMR (400 MHz, CDCl3): 6 = 8.91 (s, 1H), 2.38 ?2.26 (m, 1H), 1.34?1.14 (m, 4H) ppm; MS (ESI) mlz 244.9 [M + Hj.
With sodium ethanolate; In ethanol; at 20 - 56℃; 5-Bromo-2-cyclopropylpyrimidine was prepared by the method of Budesinsky, Z., Coll.Czech. Chem. Commun., 1949,14, 223-235. Cyclopropanecarboximidamidehydrochloride (2.5 g, 20.7 mmol) was dissolved in EtOH (4 mL), freshly prepared 4.1M"NaOEf irTEtOH (478 niC) was"~added followe'dTSy mucobrbmic aci
  • 2
  • [ 21577-50-4 ]
  • [ 57297-29-7 ]
  • [ 304902-95-2 ]
YieldReaction ConditionsOperation in experiment
72% NaH (60percent purity, 41 .9 g) is added in portions to EtOH (800 ml.) at 0 °C. The resulting mixture is warmed to ambient temperature and the cyclopropanecarboxamidine hydrochlorid (93.5 g,) is added in portions. The reaction is warmed to 50 °C and maintained at this temperature for 0.5 h and then cooled to ambient temperature before mucobromic acid (100 g) is added in EtOH while keeping the internal temperature below 55 °C. The mixture is allowed to cool to ambient temperature and stirred for additional 16 h. All solid components are removed by filtration and the resulting solution is concentrated under reduced pressure. Aq. HCI (1 mol/L) is added, the aqueous phase is washed with EtOAc (3x), the combined organic extracts are dried over MgS04 and the solid parts removed by filtration. The residue is concentrated under reduced pressure and the resulting solid titrated with (Rho Omicron. The solids are collected by filtration and dried yielding the title compound (68.0 g, yield 72 percent) as a colorless solid. 1 H NMR (400 MHz, CDCI3): delta = 8.91 (s, 1 H), 2.38 - 2.26 (m, 1 H), 1.34 - 1 .14 (m, 4H) ppm; MS (ESI) m/z 244.9 [M + H+].
 

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