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Chemical Structure| 101094-85-3 Chemical Structure| 101094-85-3

Structure of 101094-85-3

Chemical Structure| 101094-85-3

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Product Details of [ 101094-85-3 ]

CAS No. :101094-85-3
Formula : C14H10ClN3
M.W : 255.70
SMILES Code : ClC1=NN=C(CC2=CC=NC=C2)C2=C1C=CC=C2
MDL No. :MFCD00631940

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Application In Synthesis of [ 101094-85-3 ]

* 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 [ 101094-85-3 ]

[ 101094-85-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 102877-78-1 ]
  • [ 101094-85-3 ]
  • [ 325781-24-6 ]
YieldReaction ConditionsOperation in experiment
40% In butan-1-ol; at 130℃; for 18h; Example 9: Preparation of 1-[4-(4-pyridyloxy)phenylamino]-4-(4-pyridylmethyl)phthalazine [44.1] A mixture of 1-chloro-4-(4-pyridylmethyl)phthalazine (for preparation see Novartis patent WO98/35958, 11.02.98) (0.540 g, 2.11 mmol) and <strong>[102877-78-1]4-(4-aminophenoxy)pyridine</strong> (1.18 g, 6.33 mmol) in anhydrous 1-butanol (8.4 mL) was stirred under argon at 130C for 18h. The reaction mixture was quenched with saturated aqueous potassium carbonate (~50 mL) and then extracted with dichloromethane (3 x 100 mL). The combined organic phases were dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography in 7: 11: 2 v/v acetone-dichloromethane-methanol provided the title compound as an oil (0.340 g, 0.84 mmol, 40% yield). 1H-NMR (DMSO-d6) 9.26 (s, 1H), 8.58 (d, J = 8.3, 1H), 8.41 to 8.44 (m, 4H), 8.10 (d, J = 8.2, 1H), 7.90 to 8.03 (m, 4H), 7.30 (d, J = 5.9, 2H), 7.17 (d, J = 9.2, 2H), 6.91 (d, J = 5.8, 2H), 4.56 (s, 2H); MS ES 406 (M+H)+, calc. 405; TLC (1:7:12 v/v methanol-acetone-dichloromethane) Rf= 0.08.
40% In butan-1-ol; at 130℃; for 18h; EXAMPLE 9 Preparation of 1-[4-(4-pyridyloxy)phenylamino]-4-(4-pyridylmethyl)phthalazine A mixture of 1-chloro-4-(4-pyridylmethyl)phthalazine (for preparation see Novartis patent WO98135958, 11.02.98) (0.540 g, 2.11 mmol) and <strong>[102877-78-1]4-(4-aminophenoxy)pyridine</strong> (1.18 g, 6.33 mmol) in anhydrous 1-butanol (8.4 mL) was stirred under argon at 130 C. for 18 h. The reaction mixture was quenched with saturated aqueous potassium carbonate (~50 mL) and then extracted with dichloromethane (3*100 mL). The combined organic phases were dried over MgSO4, filtered, and concentrated. Purification by flash column chromatography in 7:11:2 v/v acetone-dichloromethane-methanol provided the title compound as an oil (0.340 g, 0.84 mmol, 40% yield). 1H-NMR (DMSO-d6) 9.26 (s, 1H), 8.58 (d, J=8.3, 1H), 8.41 to 8.44 (m, 4H), 8.10 (d, J=8.2, 11H), 7.90 to 8.03 (m, 4H), 7.30 (d, J=5.9, 2H), 7.17 (d, J=9.2, 2H), 6.91 (d, J=5.8, 2H), 4.56 (s, 2H); MS ES 406 (M+H)+, calc. 405; TLC (1:7:12 v/v methanol-acetone-dichloromethane) Rf=0.08.
  • 2
  • [ 106-47-8 ]
  • [ 101094-85-3 ]
  • [ 212141-54-3 ]
YieldReaction ConditionsOperation in experiment
In butan-1-ol; at 100℃; for 0.5h;Product distribution / selectivity; A mixture of 1.28 g (5 mmol) l-chloro-4-(4-pyridylmethyl)phthalazine, 0.67 g (5.25 mmol) 4-chloroaniline and 15 ml 1-butanol is heated for 0.5 h at 100 C while stirring in a nitrogen atmosphere. The mixture is then cooled to RT, filtered, and the filtrate washed with 1-butanol and ether. For purification, the crystallizate is dissolved in 40 ml of hot methanol, the solution treated with activated carbon, filtered via Hyflo Super CeI, and the filtrate evaporated to about half its original volume, resulting in the formation of a crystalline precipitate. After cooling to 0 C, filtration, washing of the filter residue with ether, and drying under HV for 8 h at 130 C, the title compound is obtained; m.p. >270 C; l H NMR (DMSO-d 6 ) 9.80-11.40 (br), 8.89-8.94 (m, IH), 8.67 (d, 2H)5 8.25-8.30 (m, IH), 8.06-8.17 (m, 2H), 7.87 (d, 2H), 7.69 (d, 2H)5 7. 49 (d, 2H), 4.81 (s, 2H); ESI-MS: (M+H) +=347.
  • 3
  • [ 20265-96-7 ]
  • [ 101094-85-3 ]
  • [ 212141-54-3 ]
YieldReaction ConditionsOperation in experiment
In ethanol; for 2h;Heating / reflux;Product distribution / selectivity; A mixture of 0.972 g (3.8 mmol) l-chloro-4-(4- pyridylmethyl)phthalazine, 0.656 g (4 mmol) 4-chloroaniline hydrochloride (Research Organics, Inc., Cleveland, Ohio, USA) and 20 ml ethanol is heated for 2 h under reflux. The reaction mixture is cooled in an ice bath, filtered, and the crystallizate washed with a little ethanol and ether. After drying under HV for 8 h at 110 C. and for 10 h at 150 C, the title compound is obtained as a result of thermal removal of HCl; m.p. >270 C; ' H NMR (DMSO-d 6 ) 9.80-11.40 (br), 8.89-8.94 (m, IH), 8.67 (d, 2H), 8.25-8.30 (m, IH), 8.06-8.17 (m, 2H), 7.87 (d, 2H), 7. 69 (d, 2H), 7.49 (d, 2H), 4.81 (s, 2H); ESI-MS: (M+H) +=347.
 

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