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Chemical Structure| 851684-46-3 Chemical Structure| 851684-46-3

Structure of 851684-46-3

Chemical Structure| 851684-46-3

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Product Details of [ 851684-46-3 ]

CAS No. :851684-46-3
Formula : C21H15Cl2FIN3O
M.W : 542.17
SMILES Code : IC1=CC2=C(NC3=CC=C(OCC4=CC=CC(F)=C4)C(Cl)=C3)N=CN=C2C=C1.[H]Cl

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Application In Synthesis of [ 851684-46-3 ]

* 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 [ 851684-46-3 ]

[ 851684-46-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 98556-31-1 ]
  • [ 202197-26-0 ]
  • [ 851684-46-3 ]
YieldReaction ConditionsOperation in experiment
70% In isopropanol; for 4h;Heating / reflux; [3-Chloro-4-(3-fluorobenzyloxy)phenyl](6-iodoquinazolin-4-yl)amine hydrochloride (15). To a suspension of 14 (12.5 g, 43.0 mmol) in 2-propanol (300 mL) was added 13 (11.2 g, 44.3 mmol). The resulting suspension was refluxed 4 hours and then the volatiles were removed under reduced pressure and the crude solid was triturated with hot acetone (400 mL) and dried at 60 C. for 2 hours to give 15 (16.4 g, 70%) as a pale yellow solid.
58% In 1,2-dichloro-ethane; tert-butyl alcohol; for 19h;Heating / reflux; 3-CHLORO-4- (3-FLUORO-BENZYLOXY)-PHENYLAMINE (3.1 g, 12 mmol) and 4-chloro-6-iodo- quinazoline (3.28 g, 11. 3 mmol) are dissolved in a 1 : 1 mixture of DCE : reaction mixture is REFLUXED for 19 hours. The product is isolated by suction filtration through sintered glass, washed with excess DCM, and air dried to afford 3.8 g (7. Ommol, 58%) of the clean desired material. <P>STEPF : (3- {4- [3-CHLORO-4- (3-FLUORO-BENZYLOXY)-PHENYLAMINO]-QUINAZOLIN-6-YL}-PROP-2-YNYL)- carbamic acid tert-butyl ester.
58% In 1,2-dichloro-ethane; tert-butyl alcohol; for 19h;Heating / reflux; Step E: [3-chloro-4-(3-fluoro-benzyloxy)-phenyl]-(6-iodo-quinazolin-4-yl)-amine hydrochloride salt. 3-Chloro-4-(3-fluoro-benzyloxy)-phenylamine (3.1 g, 12 mmol) and 4-chloro-6-iodo-quinazoline (3.28 g, 11.3 mmol) are dissolved in a 1:1 mixture of DCE:t-BuOH (56 ml). The reaction mixture is refluxed for 19 hours. The product is isolated by suction filtration through sintered glass, washed with excess DCM, and air dried to afford 3.8 g (7.0 mmol, 58%) of the clean desired material.
In water monomer; at 25 - 60℃; for 6h; KSM-01 l. lmol and KSM-02 Imole charge to the reactor followed by 15Vol water and allow to stir for 30min at 25-30C. Allow to heat for 5.5hrs at 55-60C and cool the reaction mass at 25-30C. Filter the reaction mass and suck dry well to get stage-01 of formula (P) as wet cake 2.5times (w/w). Yield: 2.15 (on dry basis w/w) HPLC purity: 99.187%.

  • 2
  • [ 568577-88-8 ]
  • [ 851684-46-3 ]
  • [ 1432450-83-3 ]
  • 3
  • [ 851684-46-3 ]
  • [ 364794-80-9 ]
  • [ 1432450-84-4 ]
  • 4
  • [ 851684-46-3 ]
  • [ 859833-22-0 ]
  • [ 1432450-91-3 ]
 

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