2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

Base Information

Chemical Name:2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester
CAS No.:872983-85-2
Molecular Formula:C₄₁H₅₇N₃O₇Si
Molecular Weight:732.005
Hs Code.:

2-[2-(2-<i>tert</i>-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(<i>tert</i>-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

Synonyms:2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

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Chemical Property of 2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

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Technology Process of 2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

There total 1 articles about 2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl 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: 65.0%

: 2-amino-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

: 108334-64-1
N-tert-butyloxycarbonyl-L-valyl-L-phenylalanine

: 872983-85-2
2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 0 ℃;
DOI:10.1016/j.bmc.2005.08.019

Reference yield: 85.0%

: 872983-85-2
2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

: 872983-86-3
2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; at 0 ℃;
DOI:10.1016/j.bmc.2005.08.019

Reference yield:

: 872983-85-2
2-[2-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-phenyl-propionylamino]-5-(tert-butyl-diphenyl-silanyloxy)-pentanoic acid methyl ester

: (2R)-2-[(2S)-2-{(2S)-2-acetylamino-3-methylbutyrylamino}-3-phenylpropionylamino]-5-hydroxypentanoic acid benzylamide

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / LiOH / tetrahydrofuran; H₂O / 0 °C

2: 57 percent / 1-hydroxy-1H-benzotriazole; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide HCl; triethylamine / CH₂Cl₂ / cooling

3: trifluoroacetic acid / CH₂Cl₂ / 0 °C

4: 0.07 g / triethylamine; 4-(dimethylamino)pyridine / CH₂Cl₂ / 0 °C

5: 91 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 20 °C

With dmap; lithium hydroxide; tetrabutyl ammonium fluoride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/j.bmc.2005.08.019