(S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate

Base Information

• Chemical Name: (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate
• CAS No.: 1351234-59-7
• Molecular Formula: C₂HF₃O₂*C₁₄H₁₈N₂O₃
• Molecular Weight: 376.332
• Mol file: 1351234-59-7.mol

Synonyms:(S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate

Chemical Property of (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate

There total 3 articles about (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate 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:

allyl 2-(4-methylphenylsulfonamido)acetate → (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate (1351234-59-7)

Guidance literature:

Multi-step reaction with 2 steps

1: PyBOP; N-ethyl-N,N-diisopropylamine / chloroform / 2 h / 23 °C / Inert atmosphere

2: dichloromethane / -10 - 23 °C / Inert atmosphere

With PyBOP; N-ethyl-N,N-diisopropylamine; In dichloromethane; chloroform;

DOI:10.1021/ol301178r

Reference yield:

N-tert-butoxycarbonyl-L-phenylalanine (13734-34-4) → (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate (1351234-59-7)

Guidance literature:

Multi-step reaction with 2 steps

1: PyBOP; N-ethyl-N,N-diisopropylamine / chloroform / 2 h / 23 °C / Inert atmosphere

2: dichloromethane / -10 - 23 °C / Inert atmosphere

With PyBOP; N-ethyl-N,N-diisopropylamine; In dichloromethane; chloroform;

DOI:10.1021/ol301178r

Reference yield:

glycine allyl ester (158840-15-4) + trifluoroacetic acid (76-05-1) → (S)-1-((2-(allyloxy)-2-oxoethyl)amino)-1-oxo-3-phenylpropan-2-aminium 2,2,2-trifluoroacetate (1351234-59-7)

Guidance literature:

In dichloromethane; at -10 - 23 ℃; Inert atmosphere;

DOI:10.1021/ol301178r

upstream raw materials:

N-tert-butoxycarbonyl-L-phenylalanine

glycine allyl ester

trifluoroacetic acid

Downstream raw materials:

allyl 2-((S)-2-((2S,3S)-3-methylaziridine-2-carboxamido)-3-phenylpropanamido)acetate

allyl 2-((S)-2-((2S,3S)-1-((S)-2-(((allyloxy)carbonyl)amino)-4-methylpentanoyl)-3-methylaziridine-2-carboxamido)-3-phenylpropanamido)acetate

(3S,9S,12S,13S)-9-benzyl-3-isobutyl-13-methyl-1,4,7,10-tetraazabicyclo[10.1.0]tridecane-2,5,8,11-tetraone

(3S,9S,12S,13S)-12-azido-9-benzyl-3-isobutyl-13-methyl-1,4,7,10-tetraazacyclotridecane-2,5,8,11-tetraone