methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Base Information

Chemical Name:methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate
CAS No.:104447-79-2
Molecular Formula:C₂₅H₂₈N₂O₄
Molecular Weight:420.508
Hs Code.:

methyl 4-<<6-<N-(cyclopentylmethyl)carbamoyl>indol-1-yl>methyl>-3-methoxybenzoate

Synonyms:methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Suppliers and Price of methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

There total 7 articles about methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate 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: 37.0%

: 104447-79-2
methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Guidance literature:

Reference yield:

: 7356-11-8
4-methyl-3-nitro-benzoic acid methyl ester

: 104447-79-2
methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / dimethylformamide / 2 h / 130 °C

2: 85 percent / H₂ / 10percent Pd/C / tetrahydrofuran / 0.58 h / 2585.7 Torr

3: 95 percent / aq. LiOH / tetrahydrofuran; methanol / 6 h / 60 °C

4: 1.) 1,1'-carbonyldiimidazole / 1.) CH₂Cl₂, reflux, 30 min, 2.) CH₂Cl₂, reflux, 30 min

5: 1.) NaH / 1.) DMF, 0 deg C, 1 h, 2.) DMF, RT, 24 h

With lithium hydroxide; hydrogen; sodium hydride; 1,1'-carbonyldiimidazole; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00091a010

Reference yield:

: 104447-80-5
(E)-1-(dimethylamino)-2-[4-(methoxycarbonyl)-2-nitrophenyl]ethene

: 104447-79-2
methyl 4-<<6-indol-1-yl>methyl>-3-methoxybenzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / H₂ / 10percent Pd/C / tetrahydrofuran / 0.58 h / 2585.7 Torr

2: 95 percent / aq. LiOH / tetrahydrofuran; methanol / 6 h / 60 °C

3: 1.) 1,1'-carbonyldiimidazole / 1.) CH₂Cl₂, reflux, 30 min, 2.) CH₂Cl₂, reflux, 30 min

4: 1.) NaH / 1.) DMF, 0 deg C, 1 h, 2.) DMF, RT, 24 h

With lithium hydroxide; hydrogen; sodium hydride; 1,1'-carbonyldiimidazole; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1021/jm00091a010