4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

Base Information

Chemical Name:4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline
CAS No.:1190391-56-0
Molecular Formula:C₂₄H₃₆N₂OSi
Molecular Weight:396.648
Hs Code.:

Synonyms:4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

Suppliers and Price of 4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

There total 1 articles about 4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline 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: 66.0%

: 1190391-55-9
benzyl {4-[(3E,5R,6R)-5-{[(benzyloxy)carbonyl]amino}-6-{[tert-butyl(dimethyl)silyl]oxy}-6-(3-chlorophenyl)-2-oxohex-3-en-1-yl]phenyl}carbamate

: 1190391-56-0
4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; for 1h;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1190391-56-0
4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

: 1190391-57-1
tert-butyl (2S,5R)-2-(4-aminobenzyl)-5-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(phenyl)methyl]pyrrolidine-1-carboxylate

: 1190391-58-2
tert-butyl (2R,5R)-2-(4-aminobenzyl)-5-[(R)-{[tert-butyl(dimethyl)silyl]oxy}(phenyl)methyl]pyrrolidine-1-carboxylate

Guidance literature:: With triethylamine; In tetrahydrofuran; optical yield given as %de;
DOI:10.1016/j.bmcl.2010.12.087

Reference yield:

: 1190391-56-0
4-({(5R)-5-[(R)-([tert-butyl(dimethyl)silyl]oxy)(phenyl)methyl]pyrrolidin-2-yl}methyl)aniline

: 1190391-85-5
(2S,5R)-tert-butyl 2-(4-aminobenzyl)-5-((R)-hydroxy(phenyl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 4 h / 20 °C

With tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2010.12.087