5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

Base Information

Chemical Name:5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide
CAS No.:1603832-29-6
Molecular Formula:C₂₃H₂₆FN₃O₂
Molecular Weight:395.477
Hs Code.:

Synonyms:5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

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Chemical Property of 5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

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Technology Process of 5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

There total 11 articles about 5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide 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: 14.0%

: 10312-83-1
methoxyacetaldehyde

: 1603833-80-2
5-piperidin-4-yl-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

: 1603832-29-6
5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

Guidance literature:: methoxyacetaldehyde; 5-piperidin-4-yl-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide; In dichloromethane; at 60 ℃; for 1h; Molecular sieve;

With sodium tris(acetoxy)borohydride; In dichloromethane; at 60 ℃; for 3h;

Reference yield:

: 1603833-77-7
5-(1-tert-butoxycarbonyl-piperidin-4-yl)-1H-indole-2-carboxylic acid ethyl ester

: 1603832-29-6
5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hydroxide; water / tetrahydrofuran / 16 h / 20 °C

2.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C

2.2: 20 °C

3.1: water; hydrogenchloride / 1,4-dioxane / 3 h / 20 - 40 °C

4.1: dichloromethane / 1 h / 60 °C / Molecular sieve

4.2: 3 h / 60 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1603833-78-8
5-(1-tert-butoxycarbonyl-piperidin-4-yl)-1H-indole-2-carboxylic acid

: 1603832-29-6
5-[1-(2-methoxy-ethyl)-piperidin-4-yl]-1H-indole-2-carboxylic acid (4-fluoro-phenyl)-amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 20 °C

2.1: water; hydrogenchloride / 1,4-dioxane / 3 h / 20 - 40 °C

3.1: dichloromethane / 1 h / 60 °C / Molecular sieve

3.2: 3 h / 60 °C

With hydrogenchloride; water; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;