4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

Base Information

Chemical Name:4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide
CAS No.:110707-84-1
Molecular Formula:C₃₂H₃₅N₃O₅S
Molecular Weight:573.713
Hs Code.:

Synonyms:4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

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Chemical Property of 4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

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Technology Process of 4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

There total 7 articles about 4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide 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: 51.0%

: 88-19-7
methyl 2-(aminosulfonyl)benzoate

: 110707-80-7
4-<<5-<(cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxybenzoic acid

: 110707-84-1
4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane;
DOI:10.1021/jm00091a010

Reference yield:

: 1670-81-1,142396-03-0
1H-Indole-5-carboxylic acid

: 110707-84-1
4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide, 4-(dimethylamino)pyridine / CH₂Cl₂ / 48 h / Ambient temperature

2: 30 percent / silver oxide / dioxane / 4 h / Heating

3: 1.) NaH / 1.) DMF, 0 deg C, 0.5 h, 2.) DMF, RT, 2 h

4: 87 percent / aq. LiOH / tetrahydrofuran; methanol / 18 h / Ambient temperature

5: 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide (WSCDI), 4-(dimethylamino)pyridine (DMAP) / CH₂Cl₂ / 36 h / Ambient temperature

With dmap; lithium hydroxide; sodium hydride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; silver(l) oxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm00055a011

Reference yield:

: 136564-69-7
1H-indole-5-carboxylic acid benzyl ester

: 110707-84-1
4-<<5-<(2-cyclopentylmethyl)carbamoyl>-1-methylindol-3-yl>methyl>-3-methoxy-N-<(2-methylphenyl)sulfonyl>benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 32 percent / dimethylformamide / 24 h / 80 °C

2: 100 percent / H₂ / 10percent Pd/C / tetrahydrofuran; methanol / 3 h / 2585.7 Torr

3: 93 percent / 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide (WSCDI), 4-(dimethylamino)pyridine (DMAP) / CH₂Cl₂ / 48 h / Ambient temperature

4: 1.) NaH / 1.) DMF, 0 deg C, 0.5 h, 2.) DMF, RT, 2 h

5: 87 percent / aq. LiOH / tetrahydrofuran; methanol / 18 h / Ambient temperature

6: 1-ethyl-3-<3-(dimethylamino)propyl>carbodiimide (WSCDI), 4-(dimethylamino)pyridine (DMAP) / CH₂Cl₂ / 36 h / Ambient temperature

With dmap; lithium hydroxide; hydrogen; sodium hydride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00055a011