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
Safety DataBack Directory
[REACH Registrations]

Active
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
148870-57-9 suppliers list
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Telephone:
Website: www.boylechem.com
Company Name: Adamas Reagent, Ltd.  
Telephone: 4006009262 13023226327
Website: http://www.tansoole.com
Company Name: XiaoGan ShenYuan ChemPharm co,ltd  
Telephone: 15527621225; 15527621225
Website: http://www.farchem.com/
Company Name: Syntechem Co.,Ltd  
Telephone:
Website: www.syntechem.com
Company Name: Guangzhou Isun Pharmaceutical Co., Ltd  
Telephone: 020-39119399 18927568969
Website: http://www.isunpharm.com
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: Shanghai YuLue Chemical Co., Ltd.  
Telephone: 021-60345187 13671753212
Website: https://www.chemicalbook.com/ShowSupplierProductsList16365/0_EN.htm
Company Name: Shanghai Kewel Chemical Co., Ltd.  
Telephone: 021-64609169 18901607656
Website: http://www.kewelchem.com/
Company Name: Nanjing Chalf-Pharm Technology Co., Ltd.  
Telephone: 025-57018978 18251899859
Website: http://www.chalf-pharm.com
Company Name: LUCKY PHARMA CO., LIMITED  
Telephone: 0571-86403260 86403970
Website: www.lkbiology.com
Company Name: Dongyang Honsen Co., Limited  
Telephone: +86-0579-86846643 18072368515
Website: www.honsentech.com.cn
Company Name: Hubei Jusheng Technology Co.,Ltd  
Telephone: 027-59599241 18871490274
Website: http://www.jushengtech.com
Company Name: Amadis Chemical Company Limited  
Telephone: 571-89925085
Website: http://www.amadischem.com
Company Name: Hubei Xinyuanshun Pharmaceutical Chemical Co., Ltd.  
Telephone: 027-50664929, 13971561712
Website: www.chemicalbook.com/ShowSupplierProductsList20057/0_EN.htm
Company Name: Beijing Xiuzheng Innovation Medicine Research Institute Co.,Ltd.  
Telephone: 010-61765302
Website: www.xiuzheng.com
Company Name: Shanghai Zhen Li Biological Technology Co., Ltd  
Telephone: 021-16621358918; 18516310516;16621358918;13045646768
Website: https://www.chemicalbook.com/ShowSupplierProductsList30395/0_EN.htm
Company Name: Capot Chemical Co.,Ltd.  
Telephone: +86-(0)57185586718 +86-13336195806
Website: www.capot.com/
Company Name: XinYao(Shenzhen) Biological Technology Co., Ltd.  
Telephone: 0755-89880280
Website: www.xinyaosz.com
Tags:148870-57-9 Related Product Information
148849-68-7 85175-52-6 155974-00-8 330786-24-8 35202-55-2 1086026-31-4 304462-60-0 1246638-08-3 93-40-3 1235547-07-5 73954-34-4 304464-97-9 85175-65-1 85175-59-3 866783-13-3 73344-75-9 60028-86-6 1204612-29-2