4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Base Information

Chemical Name:4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester
CAS No.:142535-48-6
Molecular Formula:C₃₂H₃₉N₃O₅
Molecular Weight:545.679
Hs Code.:

Synonyms:4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

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Chemical Property of 4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

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Technology Process of 4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

There total 4 articles about 4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester 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: 78.0%

: 70264-94-7
methyl 4-(bromomethyl)-3-methoxybenzoate

: 142535-46-4
3-((E)-2-Diethylcarbamoyl-vinyl)-1H-indole-6-carboxylic acid cyclopentylmethyl-amide

: 142535-48-6
4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/jm00091a010

Reference yield:

: 114085-90-4
6--3-formylindole

: 142535-48-6
4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 68 percent / dioxane / 24 h / Heating

2: 52 percent / aq. LiOH / tetrahydrofuran; methanol / 18 h / 40 °C

3: 47 percent / 4-(dimethylamino)pyridine, 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / CH₂Cl₂ / 36 h

4: 78 percent / K₂CO₃ / dimethylformamide

With dmap; lithium hydroxide; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00091a010

Reference yield:

: 142535-45-3
(E)-6--3-(2-carboxyethylidenyl)indole

: 142535-48-6
4-[6-(Cyclopentylmethyl-carbamoyl)-3-((E)-2-diethylcarbamoyl-vinyl)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 47 percent / 4-(dimethylamino)pyridine, 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / CH₂Cl₂ / 36 h

2: 78 percent / K₂CO₃ / dimethylformamide

With dmap; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00091a010