5-Bromoisoquinolin-1(2H)-one

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5-Bromoisoquinolin-1(2H)-one Basic information
Product Name:5-Bromoisoquinolin-1(2H)-one
Synonyms:5-Bromo-1(2H)-isoquinolinone;5-bromoisoquinolin-1-ol;5-Bromo-1,2-dihydro-1-oxoisoquinoline;5-Bromo-2H-isoquinolin-1-one;5-Bromoisoquinolin-1(2H);5-bromanyl-2H-isoquinolin-1-one;5-bromo-1,2-dihydroisoquinolin-1-one;1(2H)-Isoquinolinone, 5-bromo-
CAS:190777-77-6
MF:C9H6BrNO
MW:224.05
EINECS:
Product Categories:
Mol File:190777-77-6.mol
5-Bromoisoquinolin-1(2H)-one Structure
5-Bromoisoquinolin-1(2H)-one Chemical Properties
Boiling point 443.2±45.0 °C(Predicted)
density 1.620
storage temp. Sealed in dry,Room Temperature
pka12.19±0.20(Predicted)
form solid
color Light yellow to light brown
InChIInChI=1S/C9H6BrNO/c10-8-3-1-2-7-6(8)4-5-11-9(7)12/h1-5H,(H,11,12)
InChIKeyUKIWLFJYNMJPEG-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C(Br)=CC=C2)C=CN1
Safety Information
HS Code 2933499090
MSDS Information
5-Bromoisoquinolin-1(2H)-one Usage And Synthesis
Synthesis
5-BroMo-3,4-dihydroisoquinolin-1(2H)-one

1109230-25-2

5-BROMOISOQUINOLIN-1(2H)-ONE

190777-77-6

5-Bromo-3,4-dihydroisoquinolin-1(2H)-one (4.3 g, 18.9 mmol) and 2,3-dicyano-5,6-dichloro-1,4-benzoquinone (8.6 g, 37.9 mmol) were mixed in 1,4-dioxane (76 mL). The reaction mixture was stirred at 100 °C for 24 hours. Upon completion of the reaction, the solvent was removed by evaporation and the residue was dissolved in ethyl acetate (500 mL) and washed with 10% aqueous sodium hydroxide solution (2 x 500 mL). The organic and aqueous layers were separated and the aqueous layer was further extracted with ethyl acetate (4 x 300 mL). All organic layers were combined and dried with anhydrous sodium sulfate, then concentrated by evaporation. The product was purified by fast chromatography with the eluent being a solvent mixture of dichloromethane and methanol (ratio tapered from 99:1 to 96:4) to afford 5-bromoisoquinolin-1(2H)-one (1.49 g, 6.65 mmol, 35% yield) as a yellow solid. The product was analyzed by LCMS showing a purity of 94% with a retention time (Rt) of 1.243 min, and electrospray mass spectrometry (ESMS) showed a molecular ion peak m/z of 224 ([M+H]+).

References[1] Patent: WO2014/153055, 2014, A2. Location in patent: Paragraph 0120-0121
[2] Patent: WO2015/20553, 2015, A1. Location in patent: Paragraph 00113-00114
[3] Patent: WO2015/50471, 2015, A1. Location in patent: Paragraph 00107; 00108
[4] Patent: WO2015/50472, 2015, A1. Location in patent: Paragraph 00111; 00112
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