4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Base Information

Chemical Name:4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester
CAS No.:104436-02-4
Molecular Formula:C₂₄H₂₇N₃O₄
Molecular Weight:421.496
Hs Code.:

Synonyms:4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

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Chemical Property of 4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

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Technology Process of 4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

There total 5 articles about 4-[6-(3-Cyclopentyl-ureido)-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:

: 3556-83-0
methyl 4-methyl-3-methoxybenzoate

: 104436-02-4
4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / bromine / CCl₄ / 4 h / Irradiation

2: 95 percent / K₂CO₃ / acetone / 48 h / Heating

3: 95 percent / acetic acid-EtOAc, H₂ / 10percent Pd/C / 24 h / 2585.7 Torr

4: 2.) Et₃N / 1.) dioxane, RT, 30 min, 2.) 80 deg C, 2.5 h

With hydrogen; bromine; potassium carbonate; acetic acid; ethyl acetate; triethylamine; palladium on activated charcoal; In tetrachloromethane; acetone;
DOI:10.1021/jm00168a036

Reference yield:

: 7151-68-0
3-methoxy-p-toluic acid

: 104436-02-4
4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / acetyl chloride / 36 h

2: 64 percent / bromine / CCl₄ / 4 h / Irradiation

3: 95 percent / K₂CO₃ / acetone / 48 h / Heating

4: 95 percent / acetic acid-EtOAc, H₂ / 10percent Pd/C / 24 h / 2585.7 Torr

5: 2.) Et₃N / 1.) dioxane, RT, 30 min, 2.) 80 deg C, 2.5 h

With hydrogen; bromine; potassium carbonate; acetic acid; ethyl acetate; triethylamine; acetyl chloride; palladium on activated charcoal; In tetrachloromethane; acetone;
DOI:10.1021/jm00168a036

Reference yield:

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

: 104436-02-4
4-[6-(3-Cyclopentyl-ureido)-indol-1-ylmethyl]-3-methoxy-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / K₂CO₃ / acetone / 48 h / Heating

2: 95 percent / acetic acid-EtOAc, H₂ / 10percent Pd/C / 24 h / 2585.7 Torr

3: 2.) Et₃N / 1.) dioxane, RT, 30 min, 2.) 80 deg C, 2.5 h

With hydrogen; potassium carbonate; acetic acid; ethyl acetate; triethylamine; palladium on activated charcoal; In acetone;
DOI:10.1021/jm00168a036