(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

Base Information

Chemical Name:(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate
CAS No.:1242104-17-1
Molecular Formula:C₆₃H₇₃N₃O₈Si
Molecular Weight:1028.37
Hs Code.:

(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

Synonyms:(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

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Chemical Property of (2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

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Technology Process of (2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

There total 23 articles about (2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate 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: 49.0%

: 1242104-23-9
(2S,3aR,5R,6S,7aS)-6-acetoxy-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-5-yl 3-(trifluoromethyl)benzoate

: 1242104-17-1
(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

Guidance literature:: With N-methylcarbazole; cyclohexa-1,4-diene; In tetrahydrofuran; water; for 18h; Inert atmosphere; UV-irradiation;
DOI:10.1002/chem.201400046

Reference yield:

: 1621925-46-9
C₃₇H₆₀N₂O₅Si₃

: 1242104-17-1
(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; fluorosilicic acid / water; acetonitrile / 12.5 h / 20 - 65 °C

2: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C / Inert atmosphere

3: triethylamine; dmap / dichloromethane / 0.5 h / 20 °C / Inert atmosphere

4: cyclohexa-1,4-diene; N-methylcarbazole / tetrahydrofuran; water / 18 h / Inert atmosphere; UV-irradiation

With dmap; fluorosilicic acid; N-methylcarbazole; cyclohexa-1,4-diene; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; dichloromethane; water; acetonitrile;
DOI:10.1002/chem.201400046

Reference yield:

: 481072-37-1
(S)-3-(p-benzyloxyphenyl)lactic acid methyl ester

: 1242104-17-1
(2S,3aS,6R,7aS)-1-((S)-2-((S)-2-(benzyloxy)-3-(4-(benzyloxy)phenyl)propanamido)-3-phenylpropanoyl)-2-(4-(tert-butyldiphenylsilyloxy)butylcarbamoyl)octahydro-1H-indol-6-yl acetate

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydride / tetrahydrofuran / 0.25 h / 0 °C / Inert atmosphere

1.2: 1.5 h / 20 °C / Inert atmosphere

2.1: methanol; lithium hydroxide monohydrate / tetrahydrofuran; water / 3 h / 20 °C

3.1: triethylamine; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C / Inert atmosphere

4.1: methanol; lithium hydroxide monohydrate / tetrahydrofuran; water / 0.5 h / 20 °C

5.1: HATU; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 20 °C / Inert atmosphere

6.1: triethylamine; dmap / dichloromethane / 0.5 h / 20 °C / Inert atmosphere

7.1: cyclohexa-1,4-diene; N-methylcarbazole / tetrahydrofuran; water / 18 h / Inert atmosphere; UV-irradiation

With methanol; dmap; N-methylcarbazole; lithium hydroxide monohydrate; cyclohexa-1,4-diene; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; dichloromethane; water;
DOI:10.1002/chem.201400046