trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester

Base Information

• Chemical Name: trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester
• CAS No.: 221077-29-8
• Molecular Formula: C₂₀H₂₉F₃N₂O₆S
• Molecular Weight: 482.521

Synonyms:trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester

Chemical Property of trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester

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Technology Process of trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester

There total 3 articles about trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl 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: 37.0%

trifluoromethylsulfonic anhydride (358-23-6) + tert-butyl (1S)-1-(4-hydroxybenzyl)-2-oxo-2-(pentylamino)ethylcarbamate (221076-98-8) → trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester (221077-29-8)

Guidance literature:

With pyridine; In dichloromethane; at 0 ℃; for 1h;

DOI:10.1021/jm010393s

Reference yield:

Boc-Tyr-OH (3978-80-1) → trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester (221077-29-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide / CH₂Cl₂ / 23 h / 20 °C

2: 37 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

With pyridine; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane;

DOI:10.1021/jm010393s

Reference yield:

n-Pentylamine (110-58-7) → trifluoro-methanesulfonic acid 4-(2-tert-butoxycarbonylamino-2-pentylcarbamoyl-ethyl)-phenyl ester (221077-29-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide / CH₂Cl₂ / 23 h / 20 °C

2: 37 percent / pyridine / CH₂Cl₂ / 1 h / 0 °C

With pyridine; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane;

DOI:10.1021/jm010393s

upstream raw materials:

trifluoromethylsulfonic anhydride

tert-butyl (1S)-1-(4-hydroxybenzyl)-2-oxo-2-(pentylamino)ethylcarbamate

Boc-Tyr-OH

n-Pentylamine

Downstream raw materials:

[1-pentylcarbamoyl-2-(4-vinyl-phenyl)-ethyl]-carbamic acid tert-butyl ester

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