(S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester

Base Information

Chemical Name:(S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester
CAS No.:84244-87-1
Molecular Formula:C₂₀H₂₁N₃O₃
Molecular Weight:351.405
Hs Code.:

Synonyms:(S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester

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

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Chemical Property of (S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester

Chemical Property:

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Technology Process of (S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester

There total 1 articles about (S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic 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:

: 119-68-6
N-Methylanthranilic acid

: 7524-52-9,26988-71-6,5619-09-0,14907-27-8,41222-70-2,67557-19-1,109492-62-8
(S)-tryptophan methyl ester hydrochloride

: 84244-87-1
(S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester

Guidance literature:: With 4-methyl-morpholine; diphenylphosphoranyl azide; In N,N-dimethyl-formamide; for 20h; Ambient temperature;
DOI:10.1039/c39820001092

Reference yield: 91.0%

: 64-18-6
formic acid

: 84244-87-1
(S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester

: C₂₁H₂₁N₃O₄

Guidance literature:: formic acid; With acetic anhydride; for 0.166667h;

(S)-3-(1H-Indol-3-yl)-2-(2-methylamino-benzoylamino)-propionic acid methyl ester; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmc.2013.09.030