4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile

Base Information

• Chemical Name: 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile
• CAS No.: 1598416-98-8
• Molecular Formula: C₂₆H₂₉N₅O₅
• Molecular Weight: 491.547
• Mol file: 1598416-98-8.mol

Synonyms:4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile

Chemical Property of 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile

There total 11 articles about 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile 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:

4-ethenyl-6-(methyloxy)-3-quinolinecarbonitrile (872714-54-0) + methoxy-6-nitro-4-(piperidin-4-ylaminomethyl)-phenol hydrochloride → 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile (1598416-98-8)

Guidance literature:

With N,N,N',N'-tetramethylguanidine; In N,N-dimethyl-formamide; at 20 ℃; for 3h;

Reference yield:

1-(tert-butoxycarbonyl)-4-aminopiperidine (87120-72-7) → 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile (1598416-98-8)

Guidance literature:

Multi-step reaction with 3 steps

1.1: titanium(IV) isopropylate / ethanol / 0 - 20 °C

1.2: 3 h / 20 °C

2.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 0 - 20 °C

3.1: N,N,N',N'-tetramethylguanidine / N,N-dimethyl-formamide / 3 h / 20 °C

With titanium(IV) isopropylate; hydrogenchloride; N,N,N',N'-tetramethylguanidine; In 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

4-(4-hydroxy-3-methoxy-5-nitro-benzylamino)-piperidine-1-carboxylic acid tert-butyl ester (1598417-77-6) → 4-(2-(4-(4-hydroxy-3-methoxy-5-nitrobenzylamino)piperidin-1-yl)ethyl)-6-methoxyquinoline-3-carbonitrile (1598416-98-8)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 0 - 20 °C

2: N,N,N',N'-tetramethylguanidine / N,N-dimethyl-formamide / 3 h / 20 °C

With hydrogenchloride; N,N,N',N'-tetramethylguanidine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

upstream raw materials:

1-(tert-butoxycarbonyl)-4-aminopiperidine

4-(4-hydroxy-3-methoxy-5-nitro-benzylamino)-piperidine-1-carboxylic acid tert-butyl ester

isonitrovanillin

4-ethenyl-6-(methyloxy)-3-quinolinecarbonitrile