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ChemicalBook--->CAS DataBase List--->148870-57-9

148870-57-9

148870-57-9 Structure

148870-57-9 Structure
IdentificationBack Directory
[Name]

7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one
[CAS]

148870-57-9
[Synonyms]

Ivabradine int
Ivabradine Impurity g
7,8-Dimethoxy-3-(3-iodopropyl)
7,8-DiMethoxy-3-(3-iodopropyl)-1,3-dihydro-2H
3-(3-iodopropyl)-7,8-diMethoxy-1H-benzo[d]azepin-2(3H)-one
3-(3-IODOPROPYL)-7,8-DIMETHOXY-1,3-DIHYDRO-2H-3-BENZAPINE-2-ONE
7,8-DiMethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-on
1,3-Dihydro-3-(3-iodopropyl)-7,8-dimethoxy-2H-3-benzazepin-2-one
7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one
3-(3-iodopropyl)-7,8-diMethoxy-2,3-dihydro-1H-3-benzazepin-2-one
3-(3-Iodopropyl)-7,8-diMethoxy-1,3-dihydro-2H-3-benzazepin-2-one
2H-3-Benzazepin-2-one,1,3-dihydro-3-(3-iodopropyl)-7,8-dimethoxy-
7,8-dimethoxy-3- (3-iodopropyl) - 1,3-dihydro-2h-3-benzoazepine-2-one
[EINECS(EC#)]

604-658-5
[Molecular Formula]

C15H18INO3
[MDL Number]

MFCD09955403
[MOL File]

148870-57-9.mol
[Molecular Weight]

387.21
Chemical PropertiesBack Directory
[Boiling point ]

504.5±50.0 °C(Predicted)
[density ]

1.513
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

-1.23±0.20(Predicted)
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one(148870-57-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

(Z)-3-(3-chloropropyl)-7,8-diethyl-1H-benzo[d] azepin-2 (3H)-one

85175-59-3

7,8-Dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one

148870-57-9

A mixed solution of 7,8-dimethoxy-3-(3-chloropropyl)-1,3-dihydro-2H-3-benzazepin-2-one (50.00 g, 169 mmol) with sodium iodide (32.75 g, 218 mmol) in methyl isobutyl ketone (375 mL) was reacted under argon protection at 117-118 °C with stirring. The reaction process was monitored by high performance liquid chromatography (HPLC). Upon completion of the reaction, the mixture was concentrated under reduced pressure and the residue was diluted with dichloromethane (375 mL) and water (190 mL). The organic phase was separated, washed with water (190 mL) and concentrated again under reduced pressure. The resulting residue was treated with methyl tert-butyl ether (190 mL) and the resulting suspension was cooled to 0 °C. After continuous stirring at 0 °C for 1 h, the solid product was collected by filtration, washed with methyl isobutyl ether (40 mL) and dried at 23 °C/100 mbar for 2 h. The final product was obtained as 60.10 g of light yellow solid product in 92% yield.

[References]

[1] Patent: WO2014/114341, 2014, A1. Location in patent: Page/Page column 15; 16
[2] Patent: WO2014/102827, 2014, A1. Location in patent: Paragraph 0121
[3] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 17, p. 2351 - 2354
[4] Patent: WO2010/72409, 2010, A1. Location in patent: Page/Page column 19-20
[5] Patent: WO2014/20534, 2014, A1. Location in patent: Page/Page column 13
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