ChemicalBook--->CAS DataBase List--->190777-77-6

190777-77-6

190777-77-6 Structure

190777-77-6 Structure
IdentificationBack Directory
[Name]

5-BROMOISOQUINOLIN-1(2H)-ONE
[CAS]

190777-77-6
[Synonyms]

5-bromoisoquinolin-1-ol
5-Bromoisoquinolin-1(2H)
5-Bromo-2H-isoquinolin-1-one
5-BROMOISOQUINOLIN-1(2H)-ONE
5-Bromo-1(2H)-isoquinolinone
1(2H)-Isoquinolinone, 5-bromo-
5-bromanyl-2H-isoquinolin-1-one
5-bromo-1,2-dihydroisoquinolin-1-one
5-Bromo-1,2-dihydro-1-oxoisoquinoline
[Molecular Formula]

C9H6BrNO
[MDL Number]

MFCD11226915
[MOL File]

190777-77-6.mol
[Molecular Weight]

224.05
Chemical PropertiesBack Directory
[Boiling point ]

443.2±45.0 °C(Predicted)
[density ]

1.620
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

12.19±0.20(Predicted)
[color ]

Light yellow to light brown
[InChI]

InChI=1S/C9H6BrNO/c10-8-3-1-2-7-6(8)4-5-11-9(7)12/h1-5H,(H,11,12)
[InChIKey]

UKIWLFJYNMJPEG-UHFFFAOYSA-N
[SMILES]

C1(=O)C2=C(C(Br)=CC=C2)C=CN1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P309+P311
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

5-BROMOISOQUINOLIN-1(2H)-ONE(190777-77-6)1HNMR
Hazard InformationBack Directory
[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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