2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

Base Information

Chemical Name:2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid
CAS No.:1182349-07-0
Molecular Formula:C₂₆H₂₃N₃O₅
Molecular Weight:457.486
Hs Code.:

Synonyms:2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

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Chemical Property of 2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

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Technology Process of 2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

There total 1 articles about 2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic 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: 68.6%

: 1182349-15-0
2-benzyloxycarbonylamino-3-[(4-bromo-1H-indole-2-carbonyl)amino]propionic acid methyl ester

: 98-80-6
phenylboronic acid

: 1182349-07-0
2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

Guidance literature:: 2-benzyloxycarbonylamino-3-[(4-bromo-1H-indole-2-carbonyl)amino]propionic acid methyl ester; phenylboronic acid; With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In ethanol; water; toluene; Reflux;

With hydrogenchloride; water;
DOI:10.1021/jm900363q

Reference yield: 44.0%

: 1182349-07-0
2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

: 1182348-61-3
rac-2-amino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid

Guidance literature:: 2-benzyloxycarbonylamino-3-[(4-phenyl-1H-indole-2-carbonyl)amino]propionic acid; With trimethylsilyl iodide; In dichloromethane; at 0 ℃; for 1h;

With water; In ethyl acetate;
DOI:10.1021/jm900363q