ChemicalBook--->CAS DataBase List--->22245-98-3

22245-98-3

22245-98-3 Structure

22245-98-3 Structure
IdentificationBack Directory
[Name]

6-HYDROXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE
[CAS]

22245-98-3
[Synonyms]

6-HYDROXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE
3,4-Dihydro-6-hydroxyisoquinolin-1(2H)-one
1(2H)-Isoquinolinone,3,4-dihydro-6-hydroxy-
6-hydroxy-1,2,3,4-tetrahydroisoquinolin-1-one
6-Hydroxy-3,4-dihydro-1(2H)-isoquinolinone ,97%
[Molecular Formula]

C9H9NO2
[MDL Number]

MFCD08059297
[MOL File]

22245-98-3.mol
[Molecular Weight]

163.17
Chemical PropertiesBack Directory
[storage temp. ]

Storage temp. 2-8°C
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
[HS Code ]

29334900
Spectrum DetailBack Directory
[Spectrum Detail]

6-HYDROXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE(22245-98-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-METHOXY-3,4-DIHYDRO-2H-ISOQUINOLIN-1-ONE

22246-12-4

6-HYDROXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE

22245-98-3

Step 1: 6-Methoxy-3,4-dihydroisoquinolin-1(2H)-one (2.58 g, 14 mmol) was dissolved in dichloromethane at -78 °C and boron tribromide (2.7 mL, 28 mmol) was slowly added. The reaction mixture was gradually warmed to room temperature and stirred overnight. Upon completion of the reaction, the reaction was quenched with cold water and subsequently extracted with ethyl acetate. The organic phases were combined and concentrated in vacuum to remove the solvent. The crude product was purified by ISCO CombiFlash? system using silica gel column chromatography with a dichloromethane solution of 0-15% methanol as eluent to afford 6-hydroxy-3,4-dihydroisoquinolin-1-one as a light brown solid (1.8 g, 75% yield) with a melting point of 204-206 °C; mass spectrum (electrospray ionization) m/z 162.1 [M+H ]+.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 2, p. 814 - 819
[2] Patent: US2009/69300, 2009, A1. Location in patent: Page/Page column 23
[3] Journal of Medicinal Chemistry, 2012, vol. 55, # 5, p. 2452 - 2468
[4] Patent: US2003/225122, 2003, A1. Location in patent: Page 18-19
[5] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 16, p. 4727 - 4730
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