3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

Base Information

Chemical Name:3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid
CAS No.:238428-13-2
Molecular Formula:C₂₅H₂₈N₄O₄
Molecular Weight:448.522
Hs Code.:

Synonyms:3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

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Chemical Property of 3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

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Technology Process of 3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

There total 2 articles about 3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic 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: 55.0%

: 238428-11-0
benzyl 3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylate

: 238428-13-2
3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; ethyl acetate; Ambient temperature;
DOI:10.1021/jm9706325

Reference yield:

: 238428-09-6
ethyl 3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylate

: 238428-13-2
3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / titanium tetraisopropoxide / 24 h / 100 °C

2: 55 percent / H₂ / 10 percent Pd/C / ethyl acetate; ethanol / Ambient temperature

With titanium(IV) isopropylate; hydrogen; palladium on activated charcoal; In ethanol; ethyl acetate;
DOI:10.1021/jm9706325

Reference yield: 83.0%

: 3731-51-9
2-(Aminomethyl)pyridine

: 238428-13-2
3-<2-(dimethylamino)ethyl>-5-<2-(4-phenyl-4-methyl-2,5-dioxo-1-imidazolidinyl)ethyl>-1H-indole-2-carboxylic acid

: N-(2-Pyridylmethyl)-5-[2-(4-phenyl-4-methyl-2,5-dioxoimidazolidin-1-yl)ethyl]-3-[2-(dimethylamino)ethyl]-1H-indole-2-carboxamide

Guidance literature:: With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; for 3h;
DOI:10.1039/a903328i