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Chemical Structure| 287193-30-0 Chemical Structure| 287193-30-0

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Chemical Structure| 287193-30-0

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Product Details of [ 287193-30-0 ]

CAS No. :287193-30-0
Formula : C13H9Cl2N3O
M.W : 294.14
SMILES Code : O=C(NCC#CC1=CC2=C(Cl)N=CN=C2C=C1)CCl

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Application In Synthesis of [ 287193-30-0 ]

* 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 [ 287193-30-0 ]

[ 287193-30-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 98556-31-1 ]
  • [ 7458-03-9 ]
  • [ 7681-65-4 ]
  • [ 287193-30-0 ]
  • 2-Chloro-N-{3-[4-(3-methyl-4-phenoxy-phenylamino)-quinazolin-yl]-prop-2-ynyl}-acetamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
53% With diisopropylamine;Pd(PPh3)2Cl2; In tetrahydrofuran; dichloromethane; Method M: N-{3-[4-(3-Methyl-4-phenoxy-phenylamino)-quinazolin-6-yl]-prop-2-ynyl}-2-morpholin-4-yl-acetam 2-Chloro-N-[3-(4chloro-quinazolin-6-yl)-prop-2-ynyl]-acetamide: 2-Chloro-N-prop-2-ynyl-acetamide (385 mg; 2.93 mmol) and <strong>[98556-31-1]4-chloro-6-iodoquinazoline</strong> (850 mg; 1 equiv.) were dissolved in dry THF and diisopropylamine (296 mg; 0.41 ml; 1 equiv.). To this mixture was added 0.04 equivalents of copper iodide (22 mg) and Pd(PPh3)2Cl2 (82 mg). The reaction was stirred at room temperature under a nitrogen atmosphere overnight (-20 hrs). The solvent was then removed in vacuo and the residue dissolved in CH2Cl2. This solution was transferred to a separatory funnel and washed with 1* saturated NH4Cl, brine, dried over Na2SO4 and the solvent removed in vacuo. The product was purified by silica gel chromatography eluding with 1:1 hexlEtOAc and collecting fractions with an Rf=0.25. This yielded the 2-Chloro-N-[3-(4-chloro-quinazolin-6-yl)-prop-2-ynyl]-acetamide as an off white solid (454 mg; 53%). 1H NMR (400 MHz; CDCl3) δ 4.12 (2H, s), 4.40 (2H, d, J=5.2 Hz), 7.91-7.93 (1H, dd, J=2, 6.8 Hz), 8.00 (1H, d, J=8.4 Hz), 8.34 (1H, d, J=1.8 Hz), 9.03 (1H, s). Irms (M+): 294.0, 296.0, 298.1. 2-Chloro-N-{3-[4-(3-methyl-4-phenoxy-phenylamino)-quinazolin-yl]-prop-2-ynyl}-acetamide:
  • 2
  • [ 98556-31-1 ]
  • [ 7458-03-9 ]
  • [ 287193-30-0 ]
YieldReaction ConditionsOperation in experiment
53% With copper(l) iodide; diisopropylamine;bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; at 20℃; for 20h; 2-Chloro-N-[3-(4-chloro-quinazolin-6-yl)-prop-2-ynyl]-acetamide: 2-Chloro-N-prop-2-ynyl-acetamide (385 mg; 2.93 mmol) and <strong>[98556-31-1]4-chloro-6-iodoquinazoline</strong> (850 mg; 1 equiv.) were dissolved in dry THF and diisopropylamine (296 mg; 0.41 mL; 1 equiv.). To this mixture was added 0.04 equivalents of copper iodide (22 mg) and Pd(PPh3)2Cl2 (82 mg). The reaction was stirred at room temperature under a nitrogen atmosphere overnight (20 hrs). The solvent was then removed in vacuo and the residue dissolved in CH2Cl2. This solution was transferred to a separatory funnel and washed with 1×saturated NH4Cl, brine, dried over Na2SO4 and the solvent removed in vacuo. The product was purified by silica gel chromatography eluting with 1:1 Hexanes/EtOAc and collecting fractions with an Rf=0.25. 2-Chloro-N-[3-(4-chloro-quinazolin-6-yl)-prop-2-ynyl]-acetamide was obtained as an off white solid (454 mg; 53%)
53% With copper(l) iodide; diisopropylamine;bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; at 20℃; for 20h; 2-ChIoro-N- prop-2-ynyl-acetamide (385mg; 2.93 mmol) and 4-chloro-6-iodoquinazone (850 mg; 1 equiv.) were dissolved in dry THF and diisopropylamine (296 mg; 0.41 mL; 1 equiv.). To this mixture was added 0.04 equivalents of copper iodide (22 mg) and Pd(PPh3)2CI2 (82 mg). The reaction was stirred at room temperature under a nitrogen atmosphere overnight (-20 hrs). The solvent was then removed in vacuo and the residue dissolved in CH2CI2. This solution was transferred to a separatory funnel and washed with 1 x saturated NH4CI, brine, dried over Na2SO4 and the solvent removed in vacuo. The product was purified by silica gel chromatography eluting with 1 :1 Hexanes/EtOAc and collecting fractions with an Rf = 0.25. 2-Chloro-N-[3-(4-chloro-quinazolin-6-yl)-prop-2-ynyl]-acetamide was obtained as an off white solid (454 mg; 53%). 1H NMR (400 MHz; CDCI3) δ 4.12 (2H, s), 4.40 (2H, d, J = 5.2 Hz), 7.91-7.93 (1 H1 dd, J = 2, 6.8 Hz), 8.00 (1H, d, J = 8.4 Hz), 8.34 (1 H, d, J = 1.6 Hz), 9.03 (1 H, s). lrms (M+): 294.0, 296.0, 298.1.
 

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