(2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

Base Information

Chemical Name:(2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine
CAS No.:191217-13-7
Molecular Formula:C₃₅H₅₂N₄O₂Si₂
Molecular Weight:616.994
Hs Code.:

Synonyms:(2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

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Chemical Property of (2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

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Technology Process of (2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

There total 10 articles about (2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine 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: 90.0%

: 994-30-9
triethylsilyl chloride

: 191217-12-6
(2S,3S)-3-Azido-1-[(1S)-2-(tert-butyldiphenylsilyloxy)-1-methylethylamino]-4-phenylbutan-2-ol

: 191217-13-7
(2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

Guidance literature:: With 1H-imidazole; In dichloromethane; at 0 - 20 ℃; for 26h;
DOI:10.1016/S0040-4039(97)00692-8

Reference yield:

: 106727-83-7
(S)-2-(tert-Butyldiphenylsilyloxy)-1-(methyl)-ethylamine

: 191217-13-7
(2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

Guidance literature:: Multi-step reaction with 4 steps

1: 68 percent / ethanol / 96 h / Heating

2: 73 percent / imidazole / CH₂Cl₂ / 4 h / 0 - 20 °C

3: DIC / CH₂Cl₂ / 4 h / 0 °C

4: HCl; H₂O / tetrahydrofuran / 96 h / 20 °C

With 1H-imidazole; hydrogenchloride; water; dacarbazine; In tetrahydrofuran; ethanol; dichloromethane; 1: Alkylation / 2: Etherification / 3: Acylation / 4: Hydrolysis;
DOI:10.1002/(SICI)1521-3765(19990802)5:8<2241::AID-CHEM2241>3.0.CO;2-L

Reference yield:

: 140867-26-1
2(R)-<1'(S)-azido-2'-phenylethyl>oxirane

: 191217-13-7
(2S,3S)-N-[(1S)-2-(tert-Butyldiphenylsilyloxy)-1-methylethyl]-3-azido-4-phenyl-2-(triethylsilyloxy)butylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / ethanol / 96 h / Heating

2: 73 percent / imidazole / CH₂Cl₂ / 4 h / 0 - 20 °C

With 1H-imidazole; In ethanol; dichloromethane; 1: Alkylation / 2: Etherification;
DOI:10.1002/(SICI)1521-3765(19990802)5:8<2241::AID-CHEM2241>3.0.CO;2-L