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Chemical Structure| 1009827-04-6 Chemical Structure| 1009827-04-6

Structure of 1009827-04-6

Chemical Structure| 1009827-04-6

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Product Details of [ 1009827-04-6 ]

CAS No. :1009827-04-6
Formula : C7H8BrN3O2
M.W : 246.06
SMILES Code : O=C(C1=NC(NC)=NC=C1Br)OC
MDL No. :MFCD20527705

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Application In Synthesis of [ 1009827-04-6 ]

* 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 [ 1009827-04-6 ]

[ 1009827-04-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1009827-04-6 ]
  • [ 380430-55-7 ]
  • methyl 3-(methylamino)-5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
21% With sodium acetate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In N,N-dimethyl-formamide; at 120℃; for 0.166667h;Microwave; Sodium acetate (3.0 eq, 240 mg, 2.93 mmol) and 1,1'- bis(diphenylphosphino)ferrocene palladium (II) chloride (complexed with dichloromethane) (0.05 eq, 36 mg, 0.049 mmol) were added to a mixture of methyl 5- bromo-2-(methylamino)pyrimidine-4-carboxylate (1.0 eq, 240 mg, 0.975mmol), and <strong>[380430-55-7]2-amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride</strong> (1.0 eq, 226 mg, 0.98 mmol) in anydrous DMF (2 ml). The mixture was stirred under microwave heating at 1200C for 10 min. Addition of water induced precipitation of the expected compound that was filtered and dried, methyl 3-(methylamino)-5-oxo-5,6-dihydropyrimido[4,5- c]quinoline-8-carboxylate (57 mg, 21percent yield). LCMS (ES): >80percent pure, m/z 285 [M+l]+.
With sodium acetate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; In N,N-dimethyl-formamide; at 120℃; for 18.0h; Sodium acetate (3.0 eq, 240 mg, 2.93 mmol) and 1,1'-bis(diphenylphosphino)ferrocene palladium (II) chloride (complexed with dichloromethane) (0.05 eq, 36 mg, 0.049 mmol) were added to a mixture of methyl 5-bromo-2-(methylamino)pyrimidine-4-carboxylate (1.0 eq, 240 mg, 0.975 mmol), and <strong>[380430-55-7]2-amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride</strong> (1.0 eq, 226 mg, 0.98 mmol) in anhydrous DMF (2 ml). The mixture was stirred under microwave heating at 120° C. for 10 min. Addition of water induced precipitation of the expected compound that was filtered and dried. methyl 3-(methylamino)-5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate (57 mg, 21percent yield). LCMS (ES): >80percent pure, m/z 285 [M+1]+.
 

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