[(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester

Base Information

• Chemical Name: [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester
• CAS No.: 872983-25-0
• Molecular Formula: C₄₆H₅₈N₄O₆SSi
• Molecular Weight: 823.141
• Mol file: 872983-25-0.mol

Synonyms:[(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester

Chemical Property of [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester

There total 6 articles about [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]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:

2-amino-1-benzothiazol-2-yl-4-(tert-butyl-diphenyl-silanyloxy)-butan-1-ol + N-tert-butyloxycarbonyl-L-valyl-L-phenylalanine (108334-64-1) → [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester (872983-25-0)

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

DOI:10.1016/j.bmc.2005.08.019

Reference yield:

tert-butyl N-[(1R)-3-[tert-butyl(diphenyl)silyl]oxy-1-formylpropyl]carbamate (905716-08-7) → [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester (872983-25-0)

Guidance literature:

Multi-step reaction with 3 steps

1.1: n-BuLi / tetrahydrofuran / -78 °C

1.2: 0.175 g / tetrahydrofuran / 3 h / -78 °C

2.1: trifluoroacetic acid / CH₂Cl₂ / 0 °C

3.1: 0.19 g / 1-hydroxy-1H-benzotriazole; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide HCl; triethylamine / CH₂Cl₂; dimethylformamide / 0.5 h / 0 °C

With n-butyllithium; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2005.08.019

Reference yield:

(2R)-2-tert-butoxycarbamoyl-4-(tert-butyldiphenylsiloxy)butyric acid (872983-22-7) → [(1S)-1-((1S)-1-{(1R)-1-[(benzothiazol-2-yl)(hydroxy)methyl]-3-(tert-butyldiphenylsiloxy)propyl}carbamoyl)-2-methylpropyl]carbamic acid tert-butyl ester (872983-25-0)

Guidance literature:

Multi-step reaction with 5 steps

1.1: 1,1'-carbonyldiimidazole / CH₂Cl₂ / 0.5 h / 0 °C

1.2: 87 percent / triethylamine / CH₂Cl₂ / cooling

2.1: 0.2 g / LiAlH₄ / tetrahydrofuran / 2 h / 0 °C

3.1: n-BuLi / tetrahydrofuran / -78 °C

3.2: 0.175 g / tetrahydrofuran / 3 h / -78 °C

4.1: trifluoroacetic acid / CH₂Cl₂ / 0 °C

5.1: 0.19 g / 1-hydroxy-1H-benzotriazole; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide HCl; triethylamine / CH₂Cl₂; dimethylformamide / 0.5 h / 0 °C

With lithium aluminium tetrahydride; n-butyllithium; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 1,1'-carbonyldiimidazole; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2005.08.019

upstream raw materials:

N-tert-butyloxycarbonyl-L-valyl-L-phenylalanine

tert-butyl N-[(1R)-3-[tert-butyl(diphenyl)silyl]oxy-1-formylpropyl]carbamate

(2R)-2-tert-butoxycarbamoyl-4-(tert-butyldiphenylsiloxy)butyric acid

[3-(tert-butyl-diphenyl-silanyloxy)-1-(methoxy-methyl-carbamoyl)-propyl]-carbamic acid tert-butyl ester

Downstream raw materials:

((S)-1-{(S)-1-[(R)-1-(Benzothiazol-2-yl-hydroxy-methyl)-3-hydroxy-propylcarbamoyl]-2-phenyl-ethylcarbamoyl}-2-methyl-propyl)-carbamic acid tert-butyl ester

(1-{1-[1-(benzothiazole-2-carbonyl)-3-(tert-butyl-diphenyl-silanyloxy)-propylcarbamoyl]-2-phenyl-ethylcarbamoyl}-2-methyl-propyl)-carbamic acid tert-butyl ester

((S)-1-{(S)-1-[(R)-1-(Benzothiazole-2-carbonyl)-3-hydroxy-propylcarbamoyl]-2-phenyl-ethylcarbamoyl}-2-methyl-propyl)-carbamic acid tert-butyl ester