(S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

Base Information

Chemical Name:(S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester
CAS No.:119706-73-9
Molecular Formula:C₂₃H₃₉BrN₂O₄Si
Molecular Weight:515.563
Hs Code.:

Synonyms:(S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

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Chemical Property of (S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

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Technology Process of (S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

There total 9 articles about (S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl 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:

: C₃₀H₅₃BrN₂O₆Si₂

: 119706-73-9
(S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

Guidance literature:: With potassium carbonate; In tetrahydrofuran; methanol; water; Yield given;
DOI:10.1016/S0040-4039(00)80460-8

Reference yield:

: 70642-86-3
N-(tert-butoxycarbonyl)-D-tyrosine

: 119706-73-9
(S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: imidazole / dimethylformamide / 48 h

2: potassium carbonate / H₂O; methanol; tetrahydrofuran / 1 h

3: 71 percent / t-BuLi / tetrahydrofuran / -78 - 25 °C

4: 80 percent / Br₂, Hg(OAc)2 / CCl₄ / 2 h / 0 °C

5: 81 percent / DCC, Et₃N / tetrahydrofuran; 2-methyl-propan-2-ol

6: 2,6-lutidine / CH₂Cl₂

7: potassium carbonate / methanol; tetrahydrofuran; H₂O

With 1H-imidazole; 2,6-dimethylpyridine; mercury(II) diacetate; bromine; tert.-butyl lithium; potassium carbonate; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/S0040-4039(00)80460-8

Reference yield:

: 13404-22-3
tert-butyl L-alaninate hydrochloride

: 119706-73-9
(S)-2-{(R)-3-[3-Bromo-4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-methylamino-propionylamino}-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / DCC, Et₃N / tetrahydrofuran; 2-methyl-propan-2-ol

2: 2,6-lutidine / CH₂Cl₂

3: potassium carbonate / methanol; tetrahydrofuran; H₂O

With 2,6-dimethylpyridine; potassium carbonate; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1016/S0040-4039(00)80460-8