(S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

Base Information

Chemical Name:(S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one
CAS No.:1312302-82-1
Molecular Formula:C₂₈H₃₁N₃O₃S
Molecular Weight:489.638
Hs Code.:

Synonyms:(S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

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Chemical Property of (S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

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Technology Process of (S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

There total 7 articles about (S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one 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:

: 1312304-06-5
(2-{4-[5-(3,4-Dimethoxy-phenyl)-1H-indol-2-yl]-piperidin-1-yl}-2-oxo-1-thiophen-2-ylmethyl-ethyl)-(S)-carbamic acid tert-butyl ester

: 1312302-82-1
(S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

Guidance literature:: With hydrogenchloride; In diethyl ether; dichloromethane; at 20 ℃; for 3h;

Reference yield:

: 19718-49-1
4-amino-3-iodobenzoic acid methyl ester

: 1312302-82-1
(S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

Guidance literature:: Multi-step reaction with 6 steps

1: diethylamine / tetrakis(triphenylphosphine) palladium⁽⁰⁾; copper(l) iodide / 24 h / 20 °C

2: Pd(PhCN)2Cl₂ / N,N-dimethyl-formamide / 24 h / 80 °C

3: sodium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane; water / 24 h / 100 °C / Inert atmosphere

4: hydrogenchloride / dichloromethane; diethyl ether / 2 h

5: dmap; triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 22 h / 20 °C

6: hydrogenchloride / dichloromethane; diethyl ether / 3 h / 20 °C

With hydrogenchloride; dmap; sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diethylamine; triethylamine; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); Pd(PhCN)2Cl₂; In 1,4-dioxane; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1312304-03-2
tert-butyl 4-(5-bromo-1H-indol-2-yl)piperidine-1-carboxylate

: 1312302-82-1
(S)-2-amino-1-(4-(5-(3,4-dimethoxyphenyl)-1H-indol-2-yl)piperidin-1-yl)-3-(thiophen-2-yl)propan-1-one

Guidance literature:: Multi-step reaction with 4 steps

1: sodium carbonate / dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II) / 1,4-dioxane; water / 24 h / 100 °C / Inert atmosphere

2: hydrogenchloride / dichloromethane; diethyl ether / 2 h

3: dmap; triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 22 h / 20 °C

4: hydrogenchloride / dichloromethane; diethyl ether / 3 h / 20 °C

With hydrogenchloride; dmap; sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; dichloro[1,1'-bis(di-t-butylphosphino)ferrocene]palladium(II); In 1,4-dioxane; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide;