2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

Base Information

Chemical Name:2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid
CAS No.:260397-83-9
Molecular Formula:C₁₉H₂₁F₃N₂O₅
Molecular Weight:414.381
Hs Code.:

2-<i>tert</i>-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

Synonyms:2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

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Chemical Property of 2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

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Technology Process of 2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

There total 1 articles about 2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid 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: 87.0%

: 14719-21-2
trifluoroacetyl-propargyl amine

: 103882-09-3,62129-44-6
N-Boc-4-I-Phe-OH

: 260397-83-9
2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

Guidance literature:: With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/S0040-4039(00)01617-8

Reference yield: 100.0%

: 260397-83-9
2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

: 260397-84-0
3-[4-(3-amino-prop-1-ynyl)-phenyl]-2-tert-butoxycarbonylamino-propionic acid

Guidance literature:: With ammonium hydroxide; at 20 ℃;
DOI:10.1016/S0040-4039(00)01617-8

Reference yield:

: 260397-83-9
2-tert-butoxycarbonylamino-3-{4-[3-(2,2,2-trifluoro-acetylamino)-prop-1-ynyl]-phenyl}-propionic acid

: N-{3-[4-(2-amino-2-carboxy-ethyl)-phenyl]-prop-2-ynyl}-6-(6-hydroxy-3-oxo-3H-xanthen-9-yl)-isophthalamic acid; compound with trifluoro-acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / 30 percent NH₄OH / 20 °C

2: 88 percent / dimethylsulfoxide / 20 °C

3: 88 percent / H₂O / 20 °C

With ammonium hydroxide; In water; dimethyl sulfoxide;
DOI:10.1016/S0040-4039(00)01617-8