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Chemical Structure| 1227417-79-9 Chemical Structure| 1227417-79-9

Structure of 1227417-79-9

Chemical Structure| 1227417-79-9

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Product Details of [ 1227417-79-9 ]

CAS No. :1227417-79-9
Formula : C12H9ClN4O
M.W : 260.68
SMILES Code : O=C1C=C(CCl)NC2=NC(C3=CC=CC=C3)=NN12
MDL No. :MFCD18711509

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Application In Synthesis of [ 1227417-79-9 ]

* 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 [ 1227417-79-9 ]

[ 1227417-79-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 638-07-3 ]
  • [ 4922-98-9 ]
  • [ 1227417-79-9 ]
YieldReaction ConditionsOperation in experiment
67% With acetic acid; at 80℃; for 24h; Example 1; Part A; To the solution of 3-phenyl-1H-1 ,2,4-triazol-5-amine (0.8 g, 5 mmol) in acetic acid (6 mL) was added ethyl 4-chloro-3-oxobutanoate (0.75 mL, 5.5 mmol). The reaction mixture was stirred for 24 hours at 80 0C, and then cooled to room temperature. The reaction mixture was filtered. The precipitates were washed with ACN and dried to give compound 1-1 in a white powder (872 mg, 67percent yield). 1H NMR (400 MHz, CD3OD) delta 8.24-8.18 (m, 2H), 7.54-7.46 (m, 3H), 6.21 (s, 1H), 4.65 (s, 2H).; Example 6; Part A; To the solution of 3-phenyl-1 H-1 ,2,4-triazol-5-amine (0.8 g, 5 mmol) in acetic acid (6 ml_) was added ethyl 4-chloro-3-oxobutanoate (0.75 ml_, 5.5 mmol).The reaction mixture was stirred for 24 hours at 80 0C, and then cooled to room temperature. The reaction mixture was filtered. The precipitates were washed with ACN and dried to give compound 1-1 in a white powder (872 mg,67percent yield). 1H NMR (400 MHz, CD3OD) delta 8.24-8.18 (m, 2H), 7.54-7.46 (m,3H), 6.21 (s, 1 H), 4.65 (s, 2H).; Example 12; Part A; To the solution of 3-phenyl-1 H-1 ,2,4-triazol-5-amine (0.8 g, 5 mmol) in acetic acid (6 mL) was added ethyl 4-chloro-3-oxobutanoate (0.75 mL, 5.5 mmol). The reaction mixture was stirred for 24 hours at 80 0C, and then cooled to room temperature. The reaction mixture was filtered. The precipitates were washed with ACN and dried to give compound 1-1 in a white powder (872 mg, 67percent yield). 1H NMR (400 MHz, CD3OD) delta 8.24-8.18 (m, 2H), 7.54-7.46 (m, 3H), 6.21 (s, 1 H), 4.65 (s, 2H).
65.1% With acetic acid; at 80℃; <strong>[4922-98-9]3-phenyl-1H-1,2,4-triazole-5-amine</strong> (0.95 g, 5.93 mmol) obtained in Step 3-2 was dissolved in 15 mL of acetic acid and ethyl 4-chloroacetoacetate (1.07 g , 6.52 mmol), and the mixture was stirred at 80 ° C. overnight. After completion of the reaction, the precipitate was suction filtered to obtain 5-methylchloro-2-phenyl-[1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one (1.0 g, 86 mmol; yield 65.1percent)
  • 2
  • [ 1227417-79-9 ]
  • [ 18362-30-6 ]
  • [ 1227418-34-9 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In ISOPROPYLAMIDE; at 150℃; for 0.25h;Microwave irradiation; Example 30; STEP A; A reaction mixture of <strong>[18362-30-6]2-chloro-6-hydroxybenzaldehyde</strong> (31.3 mg, 0.2 mmol), compound 1-1 (26 mg, 0.1 mmol) and potassium carbonate (55 mg, 0.4 mmol) in DMA was stirred in microwave at 150 0C for 15 minutes. Compound30-1 was purified using reverse phase HPLC.
  • 3
  • [ 1227417-79-9 ]
  • [ 112270-06-1 ]
  • [ 1227416-20-7 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In ISOPROPYLAMIDE; at 90℃; for 18h; Example 47; Compound 1-1 (6.42g, 24.6 mmol) was dissolved in DMA (35 ml_) and then ethyl-2-chloro-6 hydroxybenzoate (1.1 equiv, 27.0 mmol, 5.44 g), and K2CO3 (3.0 equiv, 73.8 mmol, 10.2 g) were added and allowed to stir at 900C for 18 h. At the end of the reaction the solution was extracted with an ethyl acetate and sodium bicarbonate wash. The solid product crashed out and was filtered through a glass filter funnel with a medium pore-sized frit, and then placed under high vacuum.Compound 47-A: HPLC-MS (5 min) RT = 1.787 min, mass calculated for formula C2IH17CIN4O4 424.09, observed LCMS m/z 425.20 (M+H).
 

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