3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

Base Information

Chemical Name:3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid
CAS No.:1355150-07-0
Molecular Formula:C₃₈H₄₅N₅O₆
Molecular Weight:667.805
Hs Code.:

3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

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Chemical Property of 3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

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Technology Process of 3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

There total 5 articles about 3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid 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:

: C₄₅H₅₀N₆O₈

: 1355150-07-0
3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

Guidance literature:: With water; In acetonitrile; at 80 ℃; for 0.5h;
DOI:10.1002/cbic.201100522

Reference yield:

: 629-03-8
1 ,6-dibromohexane

: 1355150-07-0
3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate; potassium iodide / acetone / 18 h / 90 °C

2: potassium carbonate / acetonitrile / 18 h / Reflux

3: thiophenol / acetonitrile / 2 h / 80 °C

4: water / acetonitrile / 0.5 h / 80 °C

With water; potassium carbonate; thiophenol; potassium iodide; In acetone; acetonitrile; 2: Williamson reaction;
DOI:10.1002/cbic.201100522

Reference yield:

: 1355150-05-8
(4-nitrophenyl)methyl 3-{5-[(6-bromohexyl)oxy]-1H-indol-3-yl}-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoate

: 1355150-07-0
3-[5-({6-[(4-{[2-(diethylamino)ethyl]carbamoyl}phenyl)amino]-hexyl}oxy)-1H-indol-3-yl]-2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)propanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 18 h / Reflux

2: thiophenol / acetonitrile / 2 h / 80 °C

3: water / acetonitrile / 0.5 h / 80 °C

With water; potassium carbonate; thiophenol; In acetonitrile; 1: Williamson reaction;
DOI:10.1002/cbic.201100522