(R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

Base Information

Chemical Name:(R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester
CAS No.:138257-70-2
Molecular Formula:C₃₅H₄₀N₄O₈
Molecular Weight:644.725
Hs Code.:

Synonyms:(R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

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Chemical Property of (R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

Chemical Property:

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Technology Process of (R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

There total 1 articles about (R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-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:

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

: 138207-69-9,138207-70-2,138207-75-7,138207-76-8
(3S)-bis(N-benzyloxycarbonyl)-3,7-diamino-2-hydroxyheptanoic acid

: 138257-70-2
(R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

: 138257-71-3
(R)-2-((2S,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

Guidance literature:: With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; Yield given. Multistep reaction. Yields of byproduct given; 1.) THF, 0 deg C, 30 min, 2.) THF, dichloromethane, RT, 24 h;
DOI:10.1021/jm00083a013

Reference yield:

: 138257-70-2
(R)-2-((2R,3R)-3,7-Bis-benzyloxycarbonylamino-2-hydroxy-heptanoylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

: 138331-27-8
(R)-2-((2R,3R)-3,7-Diamino-2-hydroxy-heptanoylamino)-3-[1-(2-nitro-benzenesulfonyl)-1H-indol-3-yl]-propionic acid methyl ester; hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / 0.4 N HCl, H₂ / 10percent Pd/C / methanol / 1 h / 1520 Torr / Ambient temperature

2: 60 percent / 0.3 N HCl / methanol / 0.5 h / Ambient temperature

With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol;
DOI:10.1021/jm00083a013