2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

Base Information

Chemical Name:2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester
CAS No.:1026951-07-4
Molecular Formula:C₃₀H₃₀N₂O₅
Molecular Weight:498.579
Hs Code.:

2-<i>tert</i>-butoxycarbonylamino-3-(1<i>H</i>-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

Synonyms:2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl 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 2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

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Technology Process of 2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

There total 1 articles about 2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl 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:

: 5241-64-5
Boc-D-Trp-OH

: 1484-50-0
desyl bromide

: 1026951-07-4
2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

Guidance literature:: Boc-D-Trp-OH; With caesium carbonate; In ethanol; at 20 ℃; for 0.5h;

desyl bromide; In N,N-dimethyl-formamide; at 20 ℃; for 1h; Further stages.;
DOI:10.1021/jm0108449

Reference yield:

: 1026951-07-4
2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

: 361576-62-7
tert-butyl (1R)-1-(4,5-diphenyl-1H-imidazol-2-yl)-2-(1H-indol-3-yl)ethylcarbamate

Guidance literature:: With ammonium acetate; In xylene; for 0.75h; Heating;
DOI:10.1021/jm0108449

Reference yield:

: 1026951-07-4
2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid 2-oxo-1,2-diphenyl-ethyl ester

: 1,1-dibutyl-3-(4,5-diphenyl-1H-imidazol-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline

Guidance literature:: Multi-step reaction with 3 steps

1: NH₄OAc / xylene / 0.75 h / Heating

2: 71 percent / HCl(g) / ethyl acetate / 0 °C

3: 38 percent / butan-1-ol / Heating

With hydrogenchloride; ammonium acetate; In ethyl acetate; xylene; butan-1-ol; 3: Pictet-Spengler cyclization;
DOI:10.1021/jm0108449