N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate

Base Information

• Chemical Name: N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate
• CAS No.: 1152308-63-8
• Molecular Formula: C₂HF₃O₂*C₃₀H₅₀N₂O₁₁
• Molecular Weight: 728.758

Synonyms:N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate

Chemical Property of N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate

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Technology Process of N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate

There total 1 articles about N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide 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:

N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-(tert-butoxycarbonylamino)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide (946570-05-4) + trifluoroacetic acid (76-05-1) → N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate (1152308-63-8)

Guidance literature:

In dichloromethane; at 20 ℃; for 0.5h;

Reference yield:

4-acetylbenzoic acid 2,5-dioxopyrrolidin-1-yl ester (122030-76-6) + N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate (1152308-63-8) → N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-(4-acetylbenzoylamino)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide (946570-07-6)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 16h;

Reference yield:

N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide trifluoroacetate (1152308-63-8) + N-hydroxysuccinimidyl (2S)-3-(tert-butoxy)-2-(tert-butoxycarbonylamino)-propanoate (75141-72-9) → N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-((S)-3-tert-butoxy-2-(tert-butoxycarbonylamino)-propionylamino)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide (946570-11-2)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; at 20 ℃; for 72h;

upstream raw materials:

N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-(tert-butoxycarbonylamino)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide

trifluoroacetic acid

Downstream raw materials:

N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-(4-acetylbenzoylamino)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)-ethoxy)ethoxy)ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide

N-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-((S)-3-tert-butoxy-2-(tert-butoxycarbonylamino)-propionylamino)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethyl)-3-(prop-2-ynyloxy)benzoic amide

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