methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride

Base Information

• Chemical Name: methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride
• CAS No.: 129034-16-8
• Molecular Formula: C₁₂H₁₃BrN₂O₂*ClH
• Molecular Weight: 333.612
• European Community (EC) Number: 969-351-3

Synonyms:methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride;129034-16-8;methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate;hydrochloride;5-Bromo-L-tryptophan Methyl Ester Hydrochloride;SY308365;EN300-205566;methyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoatehydrochloride

Chemical Property of methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 331.99272
• Heavy Atom Count: 18
• Complexity: 288

Purity/Quality:

99% ^*data from raw suppliers

methyl2-amino-3-(5-bromo-1H-indol-3-yl)propanoatehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC(=O)C(CC1=CNC2=C1C=C(C=C2)Br)N.Cl

Technology Process of methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride

There total 2 articles about methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride 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: 100.0%

diazomethane (186581-53-3,908094-01-9,334-88-3) + 5-bromo-DL-tryptophan (6548-09-0) → methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride (129034-16-8)

Guidance literature:

With hydrogenchloride; In tetrahydrofuran; methanol; diethyl ether; at 0 ℃; for 0.0833333h;

DOI:10.1021/jm00174a008

Reference yield:

methanol (67-56-1) + 5-bromo-DL-tryptophan (6548-09-0) → methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride (129034-16-8)

Guidance literature:

With thionyl chloride; at 50 ℃; for 4h;

Reference yield: 15.0%

methyl 2-amino-3-(5-bromo-1H-indol-3-yl)propanoate hydrochloride (129034-16-8) + benzaldehyde (100-52-7) → methyl 6-bromo-1-phenyl-9H-pyrido[3,4-b]indole-3-carboxylate

Guidance literature:

With Cumene hydroperoxide; tetrabutylammomium bromide; In acetonitrile; at 70 ℃; for 15h; Green chemistry;

DOI:10.1016/j.cclet.2019.07.001

upstream raw materials:

diazomethane

5-bromo-DL-tryptophan

methanol

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