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Chemical Structure| 107558-48-5 Chemical Structure| 107558-48-5

Structure of 107558-48-5

Chemical Structure| 107558-48-5

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Product Details of [ 107558-48-5 ]

CAS No. :107558-48-5
Formula : C14H11N3O
M.W : 237.26
SMILES Code : O=C1NN=C(CC2=CC=NC=C2)C3=C1C=CC=C3
MDL No. :MFCD00443664
InChI Key :NIQMWTLRDNQDIA-UHFFFAOYSA-N
Pubchem ID :789954

Safety of [ 107558-48-5 ]

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

Application In Synthesis of [ 107558-48-5 ]

* 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 [ 107558-48-5 ]

[ 107558-48-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 106-47-8 ]
  • [ 107558-48-5 ]
  • [ 212141-54-3 ]
YieldReaction ConditionsOperation in experiment
With phosphorus pentaoxide; conc. ammonia; triethylamine hydrochloride; In chloroform; water; Example 4 1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine A mixture of 14.19 g (0.1 mol) phosphorus pentoxide, 13.77 g (0.1 mol) triethylamine hydrochloride and 12.76 g (0.1 mol) 4-chloroaniline is heated and stirred in a nitrogen atmosphere at 200 C. until a homogeneous melt has formed (about 20 min). To the melt, 5.93 g (0.025 mol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone (for preparation see German Auslegeschrift no. 1 061 788 [published 23.07.1959]) is added, and the reaction mixture is stirred for 3 h at 2000 C. After the reaction mixture has cooled to about 100 C., 200 ml of water is added. Stirring is continued until the temperature reaches about 30 C., and then 20 ml conc. ammonia (30% aqueous ammonium hydroxide solution) and 900 ml chloroform are added consecutively. As soon as a diphasic mixture has formed, the organic phase is separated off, dried over anhydrous sodium sulfate, filtered, and the filtrate evaporated on a RE to a volume of about 50 ml, to which 100 ml acetate is then added, and the mixture is cooled in an ice bath. The crystallizate obtained is filtered off and washed with acetate and ether. After recrystallization from methanol and drying under HV for 8 h at 120 C., the title compound is obtained; m.p. 194-195 C.; ESI-MS: (M+H)+=347.
With phosphorus pentaoxide; conc. ammonia; triethylamine hydrochloride; In chloroform; water; EXAMPLE 4 1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine A mixture of 14.19 g (0.1 mol) phosphorus pentoxide, 13.77 g (0.1 mol) triethylamine hydrochloride and 12.76 g (0.1 mol) 4-chloroaniline is heated and stirred in a nitrogen atmosphere at 200 C. until a homogeneous melt has formed (about 20 min). To the melt, 5.93 g (0.025 mol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone (for preparation see German Auslegeschrift no. 1 061 788 [published 23.07.1959]) is added, and the reaction mixture is stirred for 3 h at 200 C. After the reaction mixture has cooled to about 100 C., 200 ml of water is added. Stirring is continued until the temperature reaches about 30 C., and then 20 ml conc. ammonia (30% aqueous ammonium hydroxide solution) and 900 ml chloroform are added consecutively. As soon as a diphasic mixture has formed, the organic phase is separated off, dried over anhydrous sodium sulfate, filtered, and the filtrate evaporated on a RE to a volume of about 50 ml, to which 100 ml acetate is then added, and the mixture is cooled in an ice bath. The crystallizate obtained is filtered off and washed with acetate and ether. After recrystallization from methanol and drying under HV for 8 h at 120 C., the title compound is obtained; m.p. 194-195 C.; ESI-MS: (M+H)+=347.
A mixture of 14.19 g (0.1 mol) phosphorus pentoxide, 13.77 g (0.1 mol) triethylamine hydrochloride and 12.76 g (0.1 mol) 4-chloroaniline is heated and stirred in a nitrogen atmosphere at 200 C. until a homogeneous melt has formed (about 20 min). To the melt, 5.93 g (0.025 mol) 4-(4-pyridylmethyl)-l (2H)- phthalazinone (for preparation see German Auslegeschrift no. 1 061 788 [published 23.07.1959]) is added, and the reaction mixture is stirred for 3 h at 200 C. After the reaction mixture has cooled to about 100 C, 200 ml of water is added. Stirring is continued until the temperature reaches about 30 C, and then 20 ml cone, ammonia (30% aqueous ammonium hydroxide solution) and 900 ml chloroform are added consecutively. As soon as a diphasic mixture has formed, the organic phase is separated off, dried over anhydrous sodium sulfate, filtered, and the filtrate evaporated on a RE to a volume of about 50 ml, to which 100 ml acetate is then added, and the mixture is cooled in an ice bath. The crystallizate obtained is filtered off and washed with acetate and ether. After recrystallization from methanol and drying under HV for 8 h at 120 C, the title compound is obtained; m.p. 194-195 C; ESI-MS: (M+H) + =347.
Example 4 1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine A mixture of 14.19 g (0.1 mol) phosphorus pentoxide, 13.77 g (0.1 mol) triethylamine hydrochloride and 12.76 g (0.1 mol) 4-chloroaniline is heated and stirred in a nitrogen atmosphere at 200C until a homogeneous melt has formed (about 20 min). To the melt, 5.93 g (0.025 mol) 4-(4-pyridylmethyl)-1 (2H)-phthalazinone (for preparation see ]) is added, and the reaction mixture is stirred for 3 h at 200C. After the reaction mixture has cooled to about 100C, 200 ml of water is added. Stirring is continued until the temperature reaches about 30C, and then 20 ml conc. ammonia (30% aqueous ammonium hydroxide solution) and 900 ml chloroform are added consecutively. As soon as a diphasic mixture has formed, the organic phase is separated off, dried over anhydrous sodium sulfate, filtered, and the filtrate evaporated on a RE to a volume of about 50 ml, to which 100 ml acetate is then added, and the mixture is cooled in an ice bath. The crystallizate obtained is filtered off and washed with acetate and ether. After recrystallization from methanol and drying under HV for 8 h at 120C, the title compound is obtained; m.p. 194-195 C; ESI-MS: (M+H)+=347.

 

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