[4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

Base Information

Chemical Name:[4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride
CAS No.:1313040-17-3
Molecular Formula:C₂₈H₃₆N₄O₂*ClH
Molecular Weight:497.08
Hs Code.:

Synonyms:[4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

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Chemical Property of [4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

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Technology Process of [4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

There total 6 articles about [4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride 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: 98.0%

: 1313041-48-3
(3-{1-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indole-3-carbonyl]piperidin-4-yl}-benzyl)carbamic acid tert-butyl ester

: 1313040-17-3
[4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 0.416667h;

Reference yield:

: 89583-07-3
N-(2-bromoethyl)morpholine

: 1313040-17-3
[4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl acetamide / 0.5 h / 20 °C

1.2: 20 °C

2.1: N,N-dimethyl-formamide / 1 h / 0 °C

3.1: sodium hydroxide; water / 20 °C

3.2: pH 2 - 3

4.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 0.42 h / 20 °C

With hydrogenchloride; water; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In 1,4-dioxane; dichloromethane; N,N-dimethyl acetamide; N,N-dimethyl-formamide;

Reference yield:

: 933-67-5,261352-51-6
7-methyl-1H-indole

: 1313040-17-3
[4-(3-aminomethyl-phenyl)-piperidin-1-yl]-[7-methyl-1-(2-morpholin-4-yl-ethyl)-1H-indol-3-yl]-methanone hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / N,N-dimethyl acetamide / 0.5 h / 20 °C

1.2: 20 °C

2.1: N,N-dimethyl-formamide / 1 h / 0 °C

3.1: sodium hydroxide; water / 20 °C

3.2: pH 2 - 3

4.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

5.1: hydrogenchloride / 1,4-dioxane / 0.42 h / 20 °C

With hydrogenchloride; water; sodium hydride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In 1,4-dioxane; dichloromethane; N,N-dimethyl acetamide; N,N-dimethyl-formamide;