|  | |  |  | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one Basic information | 
 | Product Name: | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one |  | Synonyms: | Ivabradine Impurity 13;1,3-Dihydro-7,8-dimethoxy-2H-3-benzazepin-2-one;7,8-Dimethoxy-1H-benzo[d]azepin-2(3H)-one;7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one;2H-3-Benzazepin-2-one,1,3-dihydro-7,8-diMethoxy-;1,3-Dihydro-7,8-dimethoxybenzo[d]azepin-2-one;7,8-diMethoxy-2,3-dihydro-1H-3-benzazepin-2-one;7,8-diMethoxy-1H-benzo[d]azepin-2(3H)-one |  | CAS: | 73942-87-7 |  | MF: | C12H13NO3 |  | MW: | 219.24 |  | EINECS: | 456-160-0 |  | Product Categories: | Aromatics;Heterocycles;Intermediates |  | Mol File: | 73942-87-7.mol |  |  | 
|  |  | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one Chemical Properties | 
 | Melting point | 244.0 to 248.0 °C |  | Boiling point | 455.8±45.0 °C(Predicted) |  | density | 1.167 |  | storage temp. | Sealed in dry,Room Temperature |  | solubility | Chloroform (Slightly), DMSO (Slightly) |  | form | Solid |  | pka | 13.29±0.20(Predicted) |  | color | Off-White to Pale Beige |  | LogP | 1.23 at 23℃ and pH6.47 |  | Surface tension | 71mN/m at 36.9mg/L and 19℃ |  | CAS DataBase Reference | 73942-87-7(CAS DataBase Reference) | 
|  |  | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one Usage And Synthesis | 
 | Uses | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one is a substituted benzazepinonee derivative used in the preparation of bradycardic agents as well as isoform-selective f-current blockers. |  | Application | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one is used in the industrial preparation of pharmaceuticals and can be reacted with trifluoroacetic acid to form 3,4-dimethoxyphenylacetic acid. |  | Definition | ChEBI: 7,8-dimethoxy-1,3-dihydro-3-benzazepin-2-one is a benzazepine. |  | Synthesis | 1.Charge 142.0 g of N-(2,2-dimethoxyethyl)-2-(3,4-dimethoxyphenyl) acetamide, 710 ml of glacial acetic acid and 710 ml of conc. hydrochloric acid in a 3.0 L round bottom flask equipped with mechanical stirrer and thermometer pocket at 25°C. 2.Stir the mixture for 17 hours at 25°C.
 3.Monitor the reaction by HPLC (starting material should be less than 4.0%).
 4.Pour the reaction mixture on 3.0 kg of crushed ice, if HPLC complies.
 5.Stir the mixture for 30 minutes and filter the solid material.
 6.Wash the mixture with 1 L of water, suck dry and unload the material.
 7.Dry the 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one under vacuum at 55-60°C till the LOD comes to below 0.5%.
 
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|  |  | 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one Preparation Products And Raw materials | 
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