3-Bromo-1-methylpyridin-2(1H)-one

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3-Bromo-1-methylpyridin-2(1H)-one Basic information
Product Name:3-Bromo-1-methylpyridin-2(1H)-one
Synonyms:3-bromo-1-methyl-1,2-dihydropyridin-2-one;3-Bromo-1-methyl-1H-pyridin-2-one;3-bromo-1-methylpyridin-2-one;2(1H)-Pyridinone, 3-bromo-1-methyl-;BROMO-1-METHYLPYRIDIN-2(1H)-ONE;3-Bromo-1-methyl-2(1H)-pyridinone;3-Bromo-1-methylpyridin-2(1H)-one
CAS:81971-38-2
MF:C6H6BrNO
MW:188.02
EINECS:
Product Categories:
Mol File:81971-38-2.mol
3-Bromo-1-methylpyridin-2(1H)-one Structure
3-Bromo-1-methylpyridin-2(1H)-one Chemical Properties
Boiling point 120-125 °C(Press: 0.5 Torr)
density 1.664±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka-2.77±0.62(Predicted)
AppearanceOff-white to gray Solid
InChIInChI=1S/C6H6BrNO/c1-8-4-2-3-5(7)6(8)9/h2-4H,1H3
InChIKeyHKLQWLOMEUJSOR-UHFFFAOYSA-N
SMILESC1(=O)N(C)C=CC=C1Br
Safety Information
MSDS Information
3-Bromo-1-methylpyridin-2(1H)-one Usage And Synthesis
Synthesis
3-Bromo-2-hydroxypyridine

13466-43-8

Iodomethane

74-88-4

3-BROMO-1-METHYLPYRIDIN-2(1H)-ONE

81971-38-2

Example 19: A mixture of 3-bromo-2-hydroxypyridine (740 mg, 4.25 mmol), potassium carbonate (1.18 g, 8.5 mmol), and iodomethane (2.65 mL, 42.5 mmol) in 1,2-dimethoxyethane (DME, 10 mL) was heated to reflux, and the reaction was carried out overnight. Upon completion of the reaction, the mixture was filtered and the solids were washed with ethyl acetate. The filtrate and washings were combined and concentrated to dryness under reduced pressure. The resulting crude product was purified by dry column chromatography on silica gel (27 g) to afford the target compound 3-bromo-1-methyl-2-pyridinone (0.63 g, 79% yield) using ethyl acetate as eluent. The product was detected by low resolution mass spectrometry (LRMS, electrospray ionization, positive ion mode) and showed a molecular ion peak m/z 188 ([M + H]+).

References[1] Synlett, 2015, vol. 26, # 11, p. 1557 - 1562
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 23, p. 7076 - 7080
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 12, p. 4840 - 4860
[4] Patent: US6388084, 2002, B1
[5] Patent: WO2017/197046, 2017, A1. Location in patent: Page/Page column 344; 345
3-Bromo-1-methylpyridin-2(1H)-one Preparation Products And Raw materials
Raw materials3-Bromo-2-hydroxypyridine-->Iodomethane-->Potassium carbonate-->1,2-Dimethoxyethane
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