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

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 Structure
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
pka13.29±0.20(Predicted)
color Off-White to Pale Beige
LogP1.23 at 23℃ and pH6.47
Surface tension71mN/m at 36.9mg/L and 19℃
CAS DataBase Reference73942-87-7(CAS DataBase Reference)
Safety Information
HS Code 2914390090
MSDS Information
7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one Usage And Synthesis
Uses7,8-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.
Application7,8-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.
DefinitionChEBI: 7,8-dimethoxy-1,3-dihydro-3-benzazepin-2-one is a benzazepine.
Synthesis1.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%.
synthesis of 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one
(1S)-4,5-Dimethoxy-1-[(methylamino)methyl]benzocyclobutane hydrochloride 4,5-Dimethoxy-1-cyanobenzocyclobutane (Z)-3-(3-chloropropyl)-7,8-diethyl-1H-benzo[d] azepin-2 (3H)-one 3-(2-CHLORO-6-FLUOROBENZYL)-7,8-DIMETHOXY-1,3-DIHYDRO-2H-3-BENZAZEPIN-2-ONE BUTTPARK 31\07-18 BUTTPARK 31\07-19 7,8-DIMETHOXY-3-(4-NITROBENZYL)-1,3-DIHYDRO-2H-3-BENZAZEPIN-2-ONE BUTTPARK 31\07-17 BUTTPARK 38\07-44 BUTTPARK 31\07-25 BUTTPARK 31\07-20 BUTTPARK 38\07-43 BUTTPARK 31\07-22 7,8-Dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one BUTTPARK 31\07-21 3-(4-BROMOBENZYL)-7,8-DIMETHOXY-1,3-DIHYDRO-2H-3-BENZAZEPIN-2-ONE BUTTPARK 31\07-23 BUTTPARK 31\07-24

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