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Chemical Structure| 1007-99-4 Chemical Structure| 1007-99-4

Structure of 1007-99-4

Chemical Structure| 1007-99-4

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Product Details of [ 1007-99-4 ]

CAS No. :1007-99-4
Formula : C4H3ClN4O3
M.W : 190.54
SMILES Code : O=[N+](C1=C(O)N=C(N)N=C1Cl)[O-]
MDL No. :MFCD07367841
InChI Key :UTTPUMOOQSNOHH-UHFFFAOYSA-N
Pubchem ID :135408693

Safety of [ 1007-99-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1007-99-4 ]

* 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 [ 1007-99-4 ]

[ 1007-99-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1194-21-4 ]
  • [ 1007-99-4 ]
YieldReaction ConditionsOperation in experiment
87% With sulfuric acid; nitric acid; EXAMPLE 4 2-Amino-6-chloro-5-nitro-4(3H)-pyrimidinone A solution of 64 ml of concentrated sulfuric acid and 64 ml of concentrated nitric acid was cooled to 0° to -5° C. in an ice-salt bath, when 11.75 g (0.0807 mole) of 2-amino-6-chloro-4-(3H)-pyrimidinone were added in small portions so that the reaction temperature did not exceed 10° C. After 45 minutes, all of the starting material was added. The mixture was stirred for 3 hours at 5° C., when the mixture was poured over 400 g of ice and stirred for 1 hour at 5° C. The precipitated solids were collected by filtration and washed with 35 ml of ethanol and 35 ml of ether and dried at 20° C./2 mm Hg overnight to produce 14.7 g of a yellow solid, m.p. 268° C. The yield was 87percent. NMR, IR and MS were consistent with the expected compound. Analysis: Calculated for C4 H3 ClN4 O3.H2 O: C, 23.04; H, 2.42; N, 26.87; H2 O 8.64. Found: C, 22.70; H, 2.32; N, 26.82; H2 O (Karl Fischer), 8.48.
87% With sulfuric acid; nitric acid; In water; at 20℃; To a solution of <strong>[1194-21-4]2-amino-6-chloropyrimidin-4(3H)-one</strong> (10 g, 68.73 mmol) in H2SO4 (46 mL, 98percent) at 4O0C was added HNO3 (9 g, 65percent) dropwise with stirring. The resulting solution was stirred for an hour at room temperature. The solution was poured into 100 g of ice. A filtration was performed. The filter cake was collected and dried under an oven with reduced pressure, resulted in 12 g (87percent) of 2-amino-6-chloro-5-nitropyrimidin-4(3H)-one as a yellow solid. 1H NMR (300 MHz, DMSO-d6) delta 7.13(1H, s), 8.59 (IH, s), 12.16 (IH, s).
 

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