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2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride

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  • Chemical Name:2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride
  • CAS No.:1403385-02-3
  • Molecular Formula:C29H32ClN3O3*ClH
  • Molecular Weight:542.505
  • Hs Code.:
2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride

Synonyms:2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride

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Chemical Property of 2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride
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Technology Process of 2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride

There total 8 articles about 2-(dimethylamino)ethyl 4-{(2S,4R)-1-acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl}benzoate monohydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 8 steps
1.1: sodium tetrahydroborate; magnesium(II) chloride hexahydrate / ethanol; water / 2 h / -10 - 20 °C
2.1: pyridine / dichloromethane / 16 h / 20 °C / Inert atmosphere
3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / 1,2-dimethoxyethane; water / 6 h / 105 °C / Inert atmosphere
4.1: aluminum (III) chloride / dichloromethane / 0.33 h / 0 - 6 °C
4.2: 0.51 h / 0 °C
5.1: sodium t-butanolate / DavePhos; tris-(dibenzylideneacetone)dipalladium(0) / toluene / 16 h / 70 °C / Inert atmosphere
6.1: sodium hydroxide; water / ethanol / 2 h / 20 °C
7.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 0.08 h
7.2: 20 °C
8.1: hydrogenchloride / dichloromethane; diethyl ether / Inert atmosphere
With pyridine; hydrogenchloride; dmap; aluminum (III) chloride; sodium tetrahydroborate; magnesium(II) chloride hexahydrate; water; sodium carbonate; dicyclohexyl-carbodiimide; sodium hydroxide; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium(0); tetrakis(triphenylphosphine) palladium(0); DavePhos; In 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; toluene;
Guidance literature:
Multi-step reaction with 6 steps
1.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / 1,2-dimethoxyethane; water / 6 h / 105 °C / Inert atmosphere
2.1: aluminum (III) chloride / dichloromethane / 0.33 h / 0 - 6 °C
2.2: 0.51 h / 0 °C
3.1: sodium t-butanolate / DavePhos; tris-(dibenzylideneacetone)dipalladium(0) / toluene / 16 h / 70 °C / Inert atmosphere
4.1: sodium hydroxide; water / ethanol / 2 h / 20 °C
5.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 0.08 h
5.2: 20 °C
6.1: hydrogenchloride / dichloromethane; diethyl ether / Inert atmosphere
With hydrogenchloride; dmap; aluminum (III) chloride; water; sodium carbonate; dicyclohexyl-carbodiimide; sodium hydroxide; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium(0); tetrakis(triphenylphosphine) palladium(0); DavePhos; In 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; toluene;
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