N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester

Base Information

Chemical Name:N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester
CAS No.:1350559-61-3
Molecular Formula:C₂₄H₃₂N₄O₅S
Molecular Weight:488.608
Hs Code.:

N<sup>α</sup>-4-ethynylbenzoyl-N<sup>ε</sup>-thioacetyl-lysinyl-alaninyl-alanine methyl ester

Synonyms:N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine 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 N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester

Chemical Property:

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Technology Process of N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester

There total 4 articles about N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine 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:

: 10602-00-3
4-Ethynyl-benzoic acid

: 1350559-61-3
N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester

Guidance literature:: In tetrahydrofuran; ethyl acetate;

Reference yield:

: 75867-41-3
4-trimethylsilanylethynyl-benzoic acid methyl ester

: 1350559-61-3
N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / methanol

2: tetrahydrofuran; ethyl acetate

With hydrogenchloride; In tetrahydrofuran; methanol; ethyl acetate;

Reference yield:

: 586-76-5
4-Bromobenzoic acid

: 1350559-61-3
N^α-4-ethynylbenzoyl-N^ε-thioacetyl-lysinyl-alaninyl-alanine methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: sulfuric acid / methanol

2: triethylamine / tetrahydrofuran; cyclohexane; ethyl acetate

3: hydrogenchloride / methanol

4: tetrahydrofuran; ethyl acetate

With hydrogenchloride; sulfuric acid; triethylamine; In tetrahydrofuran; methanol; cyclohexane; ethyl acetate;