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Chemical Structure| 7024-58-0 Chemical Structure| 7024-58-0

Structure of 7024-58-0

Chemical Structure| 7024-58-0

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Product Details of [ 7024-58-0 ]

CAS No. :7024-58-0
Formula : C7H8N2O2
M.W : 152.15
SMILES Code : OC1=NC(C2CC2)=NC(O)=C1
MDL No. :MFCD19105241

Safety of [ 7024-58-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 7024-58-0 ]

* 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 [ 7024-58-0 ]

[ 7024-58-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 7024-58-0 ]
  • [ 7043-09-6 ]
YieldReaction ConditionsOperation in experiment
61% Step 2: 4,6-dichloro-2-cyclopropylpyrimidine; 1.34 g (8.40 mmol) 2-cyclopropylpyrimidine-4,6-diol and 15.0 mL (163.37 mmol) phosphorus oxychloride were boiled for 2 h. The reaction mixture was poured onto ice water and made alkaline with NaOH. The precipitate formed was suction filtered, washed and dried.Yield: 1.02 g (61% of theory)Rt(HPLC): 1.57 min (method B)
With trichlorophosphate; at 20 - 100℃; for 2.0h; To 2-cyclopropylpynmidine-4,6-diol (0.750 g, 4.93 mmol) was added phosphoryl trichloride (9.0 mL) at RT. The reaction mixture was stirred at 100 C for 2 h. The resulting solution was cooled and quenched with ice and water (20 mL) and was extracted with ethyl acetate (3 x 40 mL). The combined organic extracts were washed with brine (3 x 20 mL), dried with anhydrous Na2S(>4, and filtered. The filtrate was concentrated under reduced pressure. The title compound was obtained as a liquid and was used in the next step without further purification. MS = 189.1/191.1 (M+l).
  • 2
  • [ 57297-29-7 ]
  • [ 105-53-3 ]
  • [ 7024-58-0 ]
YieldReaction ConditionsOperation in experiment
96% 2-Cyclopropylpyrimidine-4,6-diol (2) Sodium metal (5.83 g, 254 mmol) was added to anhydrous methanol (100 mL) cooled in an ice bath. Once sodium methoxide formation was complete (all sodium dissolved), cyclopropyl carboxamidine hydrochloride (10.0 g, 80 mmol) was added and reaction mixture was stirred for 15 min. Diethyl malonate (12.6 imL, 82.9 mmol) was added dropwise and the reaction mixture was warmed to RT and stirred overnight. The suspension was then concentrated under vacuum. The resulting residue was dissolved in water and the solution was acidified with concentrated HCI to pH 5. The resulting precipitate was collected via filtration and washed sequentially with water, ether, isopropanol, and finally ether. The solid was then dried under vacuum to afford 11 .69 g (96 percent) of 2-cyclopropylpyrimidine-4,6- diol (2). LCMS m/z 153.4 (M+1 ). H NMR (400 MHz, DMSO-d6) delta 1 1 .87 (s, 2H), 5.03 (s, 1 H), 1.86 (m, 1 H), 0.98 (m, 4H).
  • 3
  • [ 57297-29-7 ]
  • [ 108-59-8 ]
  • [ 7024-58-0 ]
YieldReaction ConditionsOperation in experiment
64% With sodium methylate; for 1.25h;Reflux; Inert atmosphere; Intermediate 326-(6-chloro-2-cyclopropylpyrimidin-4-yloxy)-4-methylbenzo[d]oxazol-2(3H)-one Step 1: 2-cyclopropylpyrimidine-4,6-diol; Under a nitrogen atmosphere 1.50 mL (13.06 mmol) dimethylmalonat, 1.60 g (13.27 mmol) <strong>[57297-29-7]cyclopropanecarboxamidine hydrochloride</strong> and 15.0 mL (80.80 mmol) sodium methoxide solution (30percent) were refluxed for 1.25 h with stirring. The reaction mixture was slightly acidified and the precipitate formed was suction filtered, washed and dried.Yield: 1.35 g (64percent of theory)ESI-MS: m/z=153 (M+H)+ Rt(HPLC): 0.75 min (method K)
With sodium methylate; In methanol; at 20 - 60℃; for 18h; Cyclopropanecarboximidamide hydrochloride (2.00 g, 16.6 mmol) was added to a solution of NaOMe (2.24 g, 41.5 mmol) in MeOH (10.0 mL) at RT. To the mixture was added dimethyl malonate (2.63 g, 19.9 mmol). The reaction mixture was stirred at 60 °C for 18 h. The reaction mixture was cooled to RT, diluted with water (20 mL) and extracted with ethyl acetate (3 x 40 mL). The combined organic extracts were washed with brine (3 x 20 mL), dried with anhydrous Na2SC>4 and filtered. The filtrate was concentrated under reduced pressure. The title compound was obtained as a solid and was used for the next step without further purification. NMR (300 MHz, DMSO-de) delta: 12.45-11.02 (br, 2H), 5.11 (s, 1H), 1.96-1.87 (m, 1H), 1.03-0.98 (m, 4H).
 

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