ChemicalBook--->CAS DataBase List--->99455-01-3

99455-01-3

99455-01-3 Structure

99455-01-3 Structure
IdentificationBack Directory
[Name]

6-Iodo-1H-quinolin-2-one
[CAS]

99455-01-3
[Synonyms]

6-Iodoquinolin-2-o
6-Iodoquinolin-2-ol
6-Iodo-2(1H)- quinolone
6-iodo-2(1H)-Quinolinone
6-Iodo-1H-quinolin-2-one
[Molecular Formula]

C9H6INO
[MDL Number]

MFCD15144678
[MOL File]

99455-01-3.mol
[Molecular Weight]

271.05
Chemical PropertiesBack Directory
[Melting point ]

260-263 °C
[Boiling point ]

413.1±45.0 °C(Predicted)
[density ]

1.880
[storage temp. ]

2-8°C(protect from light)
[pka]

10.92±0.70(Predicted)
[Appearance]

Yellow to brown Solid
Safety DataBack Directory
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

6-Iodo-1H-quinolin-2-one(99455-01-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Propenamide, 3-ethoxy-N-(4-iodophenyl)-, (2E)-

99465-20-0

6-Iodo-1H-quinolin-2-one

99455-01-3

(2E)-3-(ethoxy)-N-(4-iodophenyl)-2-acrylamide (33 g, 104 mmol) was added batchwise to stirred concentrated sulfuric acid (300 mL) at 0 °C. The reaction mixture was stirred continuously for 2 hours at room temperature. Subsequently, the reaction mixture was quenched by slowly pouring it into about 1 kg of ice. The resulting solid product was collected by filtration and washed sequentially with water (3 times) and acetonitrile (2 times). Finally, the solid was dried under vacuum to afford 6-iodo-2-hydroxyquinoline as an off-white solid (27.1 g, yield: 96%). The structure of the product was confirmed by 1H NMR (400 MHz, chloroform-d) and ES-LCMS: 1H NMR δ= 6.73 (d, J = 9.6Hz, 1H), 7.17 (d, J = 8.8Hz, 1H), 7.74 (d, J = 9.6Hz, 1H), 7.77 (dd, J = 8.8,1.4Hz, 1H), 7.93 ( d, J = 1.4 Hz, 1H); ES-LCMS: m/z 272 (M + 1).

[References]

[1] Patent: WO2012/37108, 2012, A1. Location in patent: Page/Page column 134
[2] Patent: US2006/63804, 2006, A1. Location in patent: Page/Page column 9
[3] Journal of Medicinal Chemistry, 1988, vol. 31, # 10, p. 2048 - 2056
[4] Patent: US4728654, 1988, A
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