N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide

Base Information

• Chemical Name: N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide
• CAS No.: 223521-24-2
• Molecular Formula: C₂₉H₃₆FN₅O₂
• Molecular Weight: 505.636
• Mol file: 223521-24-2.mol

Synonyms:N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide

Chemical Property of N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide

There total 4 articles about N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide 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: 77.0%

4-[2-((3'-bromo)propionamido)ethyl]-1-(2-methoxyphenyl)piperazine (223521-46-8) + 6-fluoro-3-(1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indole (180161-14-2) → N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide (223521-24-2)

Guidance literature:

With triethylamine; In isopropyl alcohol; toluene; for 14h; Heating / reflux;

Reference yield:

1-(2-aminoethyl)-4-(2-methoxyphenyl)piperazine (40255-48-9) → N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide (223521-24-2)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 1 h / 0 - 20 °C

2: triethylamine / isopropyl alcohol; toluene / 14 h / Heating / reflux

With pyridine; triethylamine; In dichloromethane; isopropyl alcohol; toluene;

Reference yield:

1-(2-Methoxyphenyl)piperazine (35386-24-4) → N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)propanamide (223521-24-2)

Guidance literature:

Multi-step reaction with 4 steps

1: potassium carbonate / DMF (N,N-dimethyl-formamide); acetonitrile / 8 h / Heating / reflux

2: hydrazine / ethanol; water / 18 h / 20 °C

3: pyridine / dichloromethane / 1 h / 0 - 20 °C

4: triethylamine / isopropyl alcohol; toluene / 14 h / Heating / reflux

With pyridine; potassium carbonate; triethylamine; hydrazine; In DMF (N,N-dimethyl-formamide); ethanol; dichloromethane; water; isopropyl alcohol; toluene; acetonitrile;

upstream raw materials:

4-[2-((3'-bromo)propionamido)ethyl]-1-(2-methoxyphenyl)piperazine

6-fluoro-3-(1,2,3,6-tetrahydro-pyridin-4-yl)-1H-indole

N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]phthalimide

1-(2-Methoxyphenyl)piperazine

Downstream raw materials:

N-(2-(4-(2-methoxyphenyl)piperazin-1-yl)eth-1-yl)-N-3-(4-(6-fluoroindol-3-yl)-1,2,3,6-tetrahydropyridin-1-yl)prop-1-ylamine