4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

Base Information

Chemical Name:4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester
CAS No.:1174681-03-8
Molecular Formula:C₃₂H₄₁N₅O₅S
Molecular Weight:607.774
Hs Code.:

Synonyms:4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

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Chemical Property of 4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

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Technology Process of 4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

There total 1 articles about 4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester 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:

Reference yield:

: 865980-54-7,898265-48-0
4-amino-adamantane-1-carboxylic acid methyl ester

: 32315-10-9
bis(trichloromethyl) carbonate

: 1174681-21-0
1-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-1,2,3,4-tetrahydro-quinoxaline

: 1174681-03-8
4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

Guidance literature:: bis(trichloromethyl) carbonate; 1-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-1,2,3,4-tetrahydro-quinoxaline; With triethylamine; In dichloromethane; at 0 - 20 ℃; for 4h; Inert atmosphere;

4-amino-adamantane-1-carboxylic acid methyl ester; In dichloromethane; N,N-dimethyl-formamide; for 18h; Inert atmosphere;

Reference yield:

: 1174681-03-8
4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

: trans-4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid (5-(hydroxymethyl)adamantan-2-yl)amide

Guidance literature:: 4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester; With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; at 0 - 20 ℃; for 2h;

With water; In tetrahydrofuran; diethyl ether; ethyl acetate;

Reference yield:

: 1174681-03-8
4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester

: trans-4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid

Guidance literature:: 4-({4-[4-(4-(methanesulphonyl)piperazin-1-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carbonyl}amino)adamantane-1-carboxylic acid methyl ester; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; for 18.33h;

With hydrogenchloride; In dichloromethane; water; pH=1;