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Chemical Structure| 320337-14-2 Chemical Structure| 320337-14-2

Structure of 320337-14-2

Chemical Structure| 320337-14-2

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Product Details of [ 320337-14-2 ]

CAS No. :320337-14-2
Formula : C13H11BrFNO
M.W : 296.14
SMILES Code : NC1=CC=C(OCC2=CC=CC(F)=C2)C(Br)=C1
MDL No. :MFCD27924215

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Application In Synthesis of [ 320337-14-2 ]

* 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 [ 320337-14-2 ]

[ 320337-14-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 98556-31-1 ]
  • [ 320337-14-2 ]
  • [ 320337-18-6 ]
YieldReaction ConditionsOperation in experiment
In isopropyl alcohol; for 12h;Reflux; Step C: N-(4-(3-fluorobenzyloxy)-3-bromophenyl)-6-iodoquinazolin-4-amine (compound 14.3)[0149] 4-(3-fluorobenzyloxy)-3-bromobenzenamine (1.48 g, 5 mmol) and 4-chloro-6-iodo- quinazoline (1.45 g, 5 mmol) were dissolved in isopropanol (50 ml). The reaction mixture was refluxed for 12 hours. The solid product was collected by filtration, washed with cold isopropanol (10 mL) and ether (20 mL), and air dried to afford 2.7 g of the clean desired material.
In acetonitrile;Reflux; General procedure: (A) Reaction of an Amine with a Bicyclic Species Containing a 4-chloropyrimidine or 4-chloropyridine Ring; The optionally substituted bicyclic species and the specified amine were mixed in an appropriate solvent (typically acetonitrile unless otherwise specified, although ethanol, 2-propanol or DMSO may also be used), and heated to reflux. When the reaction was complete (as judged by tlc), the reaction mixture was allowed to cool. The resulting suspension was diluted, e.g. with acetone, and the solid collected by filtration, washing e.g. with excess acetone, and dried at 60 C. in vacuo, giving the product as the hydrochloride salt. If the free base was required (e.g. for further reaction), this was obtained by treatment with a base e.g. triethylamine; purification by chromatography was then performed if required.; The title compound was prepared according to Procedure A from 3-bromo-4-(3-fluorobenzyloxy)-aniline (0.79 g, 2.7 mmol) and <strong>[98556-31-1]4-chloro-6-iodoquinazoline</strong> (0.8 g, 2.7 mmol). 1H NMR (DMSO-d6) δ 11.1 (bs, 1H); 9.10 (s, 1H); 8.87 (s, 1H); 8.29 (d, 1H); 8.03 (s, 1H); 7.68 (m, 1H); 7.62 (d, 1H); 7.45 (m, 1H); 7.33-7.26 (m, 3H); 7.16 (m, 1H); 5.28 (s, 2H).
  • 2
  • [ 456-47-3 ]
  • [ 5847-59-6 ]
  • [ 320337-14-2 ]
  • 3
  • [ 5847-59-6 ]
  • [ 320337-14-2 ]
 

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