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Chemical Structure| 1455091-21-0 Chemical Structure| 1455091-21-0

Structure of 1455091-21-0

Chemical Structure| 1455091-21-0

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Product Details of [ 1455091-21-0 ]

CAS No. :1455091-21-0
Formula : C17H12BrNO4
M.W : 374.19
SMILES Code : O=C(C1=C(O)C2=C(C(Br)=N1)C=C(OC3=CC=CC=C3)C=C2)OC
MDL No. :MFCD29075437

Safety of [ 1455091-21-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1455091-21-0 ]

* 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 [ 1455091-21-0 ]

[ 1455091-21-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1455091-10-7 ]
  • [ 1455091-21-0 ]
YieldReaction ConditionsOperation in experiment
90.7% With N-Bromosuccinimide; In dichloromethane; for 2h; Add dichloromethane (2L) and <strong>[1455091-10-7]4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester</strong> (200.00g, 0.68mol) to the reaction flask in sequence, after stirring,Add N-bromosuccinimide (NBS) (126.60g, 0.71mol) into the reaction bottle, and after the end of the addition, react for 2 hours.After distilling off about half of the methylene chloride under reduced pressure, methanol (2L) was added, and the crystal was stirred for 1h.After filtration, the filter cake was blow-dried to obtain 1-bromo-<strong>[1455091-10-7]4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester</strong> (229.67g, yield 90.7%, purity 98.98%).
86.4% With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In methanol; at 5℃;Reflux; Methyl 4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (Compound A) 2.95 g,The stirring temperature of the ice water bath was lowered to 5-10 C, and 1.57 g of 1,3-dibromo-5,5-dimethylhydantoin was added, and methanol was used as a solvent, and the reaction was refluxed for 4-6 h.The TLC monitors the reaction to the starting material completely, 0~10 C, suction filtration, the filter cake is rinsed with methanol, and dried under vacuum.A pale yellow solid, Compound B (yield 86.4%, purity 98.5%) was obtained.
58% With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 1h;Reflux; A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (6.0 g, 20.32 mmol), N-bromosuccinimide (3.80 g, 21.33 mmol) and benzoyl peroxide (246 mg, 1.01 mmol) in CCI4 was refluxed for 1 h. Solid was filtered off through a plug of silica gel. Filtrate was concentrated and purified by silica chromatography, eluting with EtOAc. All fractions contain the desired product was combined and concentrated. Residue was suspended in 150 mL of (3/1) MeOH/EtOAc and was refluxed for 1 h. After cooled, solid was collected, rinsed with MeOH and dried on vacuo to provide the title compound 4.42 g (1 1.8 mmol) in 58% yield as a white solid. H NMR in CDC13, delta ppm: 1 1.7 (s, 1 H), 8.36 (d, 1 H, J = 9.2 Hz), 7.63 (d, 1 H, J = 2.4 Hz), 7.55-7.10 (m, 6 H), 4.06 (s, 3 H).
  • 2
  • [ 57830-14-5 ]
  • [ 1455091-21-0 ]
 

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