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4-BROMO-2-METHYLISOINDOLIN-1-ONE

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Products Intro: Product Name:4-BROMO-2-METHYLISOINDOLIN-1-ONE
CAS:435273-55-5
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G
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Products Intro: Product Name: 4-BROMO-2-METHYLISOINDOLIN-1-ONE
CAS:435273-55-5
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Products Intro: Product Name:4-Bromo-2-methylisoindolin-1-one
CAS:435273-55-5
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Products Intro: Product Name:4-Bromo-2-methylisoindolin-1-one
CAS:435273-55-5
Purity:97% Package:10g;50g;100g;
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Products Intro: Product Name:4-Bromo-2-methylisoindolin-1-one
CAS:435273-55-5
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4-BROMO-2-METHYLISOINDOLIN-1-ONE manufacturers

4-BROMO-2-METHYLISOINDOLIN-1-ONE Basic information
Product Name:4-BROMO-2-METHYLISOINDOLIN-1-ONE
Synonyms:4-BROMO-2-METHYLISOINDOLIN-1-ONE;1H-Isoindol-1-one,4-bromo-2,3-dihydro-2-methyl-;4-Bromo-2,3-dihydro-2-methyl-1H-isoindol-1-one, 4-Bromo-2,3-dihydro-2-methyl-1-oxo-1H-isoindole;4-broMo-2-Methyl-2,3-dihydro-1H-isoindol-1-one;4-(1-Methoxypropan-2-yloxy)aniline;4-Bromo-2-methyl-2,3-dihydro-isoindol-1-one;4-bromo-2-methyl-3H-isoindol-1-one;4-Bromo-2,3-dihydro-2-methyl-1H-isoindol-1-one
CAS:435273-55-5
MF:C9H8BrNO
MW:226.07
EINECS:
Product Categories:
Mol File:435273-55-5.mol
4-BROMO-2-METHYLISOINDOLIN-1-ONE Structure
4-BROMO-2-METHYLISOINDOLIN-1-ONE Chemical Properties
Boiling point 356.6±42.0 °C(Predicted)
density 1.589
storage temp. 2-8°C
form solid
pka-2.13±0.20(Predicted)
color Yellow
Safety Information
HS Code 2933790090
MSDS Information
4-BROMO-2-METHYLISOINDOLIN-1-ONE Usage And Synthesis
Synthesis
Methylamine

74-89-5

Methyl 3-bromo-2-bromomethylbenzoate

337536-14-8

4-BROMO-2-METHYLISOINDOLIN-1-ONE

435273-55-5

Methyl 3-bromo-2-(bromomethyl)benzoate (5.27 g, 17 mmol) obtained in Step 2 was dissolved in 50 mL of tetrahydrofuran and 40% aqueous methylamine solution (7.5 mL, 86 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the solvent was evaporated under reduced pressure. The resulting residue was diluted with water and extracted with ethyl acetate. The organic layers were combined, washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. After filtration, the solvent was removed by concentration under reduced pressure. The residue was purified by silica gel column chromatography to afford 4-bromo-2-methylisoindolin-1-one (3.36 g, 87% yield).1H NMR (300 MHz, CDCl3) δ 7.68 (d, 1H, J = 7.9 Hz), 7.53 (dd, 1H, J = 7.9, 0.9 Hz), 7.26 (t, 1H, J = 7.9 Hz), 7.26 (t, 1H, J = 7.9 Hz) 4.20 (s, 2H), 3.11 (s, 3H).

References[1] Patent: WO2009/51417, 2009, A2. Location in patent: Page/Page column 13
[2] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 11, p. 3036 - 3040
[3] Patent: WO2012/74951, 2012, A1. Location in patent: Page/Page column 36-37
4-BROMO-2-METHYLISOINDOLIN-1-ONE Preparation Products And Raw materials
Raw materialsMethylamine-->Methyl 3-bromo-2-bromomethylbenzoate
Tag:4-BROMO-2-METHYLISOINDOLIN-1-ONE(435273-55-5) Related Product Information
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