[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester
CAS No.:149976-33-0
Molecular Formula:C₃₄H₄₉N₃O₅Si
Molecular Weight:607.866
Hs Code.:

Synonyms:[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

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Chemical Property of [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

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Technology Process of [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

There total 1 articles about [(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic 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: 60.0%

: 87988-94-1
4-amino-5-methylisoxazole

: 98818-51-0
N-(1,1-dimethylethoxycarbonyl)-5(S)-amino-4(S)-(t-butyldimethylsilyloxy)-6-phenyl-2(R)-(phenylmethyl)hexanoic acid

: 149976-33-0
[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; for 24h; Ambient temperature;
DOI:10.1021/jm00045a015

Reference yield:

: 149976-33-0
[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

: 150348-82-6
[(1S,2S,4R)-4-(5-Acetyl-1H-imidazol-2-yl)-1-benzyl-2-hydroxy-5-phenyl-pentyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) H₂, 2.) NaOH / 1.) 10percent Pd/C / 1.) EtOH, 5 h, 2.) EtOH, reflux, overnight

2: 84 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 5 h / 50 °C

With sodium hydroxide; tetrabutyl ammonium fluoride; hydrogen; palladium on activated charcoal; In tetrahydrofuran;
DOI:10.1021/jm00045a015

Reference yield:

: 149976-33-0
[(1S,2S,4R)-1-Benzyl-2-(tert-butyl-dimethyl-silanyloxy)-4-(5-methyl-isoxazol-4-ylcarbamoyl)-5-phenyl-pentyl]-carbamic acid tert-butyl ester

: {(1S,2S,4R)-1-Benzyl-2-hydroxy-4-[5-(1-hydroxy-ethyl)-1H-imidazol-2-yl]-5-phenyl-pentyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) H₂, 2.) NaOH / 1.) 10percent Pd/C / 1.) EtOH, 5 h, 2.) EtOH, reflux, overnight

2: 84 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 5 h / 50 °C

3: 78 percent / NaBH₄ / ethanol / 0.25 h

With sodium hydroxide; sodium tetrahydroborate; tetrabutyl ammonium fluoride; hydrogen; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00045a015