N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester

Base Information

Chemical Name:N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester
CAS No.:872983-47-6
Molecular Formula:C₄₄H₅₆N₄O₆Si
Molecular Weight:765.037
Hs Code.:

Synonyms:N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester

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Chemical Property of N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester

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Technology Process of N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester

There total 7 articles about N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl 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:

: 872983-37-4
2-amino-2-(2-hydroxy-ethyl)-pent-4-enoic acid

: 872983-47-6
N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: H₂ / Pd-C / methanol / 14 h / 20 °C

2: 2.4 g / hydrochloric acid / 16 h / Heating

3: 90 percent / 2-phenylbenzoxazole; ethyldiisopropylamine / CH₂Cl₂ / 0 °C

4: 1.22 g / lithium hydroxide / tetrahydrofuran; H₂O / 0 °C

5: 1.63 g / imidazole / CH₂Cl₂ / 0 °C

6: 1.55 g / 1-hydroxy-1H-benzotriazole; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide HCl; triethylamine / CH₂Cl₂ / 0 °C

With 1H-imidazole; hydrogenchloride; lithium hydroxide; 2-phenylbenzo[d]oxazole; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1016/j.bmc.2005.08.019

Reference yield:

: C₁₆H₂₈NO₄S⁽¹⁺⁾*BF₄^(1-)

: 872983-47-6
N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: sodium hydroxide / 16 h / Heating

2: H₂ / Pd-C / methanol / 14 h / 20 °C

3: 2.4 g / hydrochloric acid / 16 h / Heating

4: 90 percent / 2-phenylbenzoxazole; ethyldiisopropylamine / CH₂Cl₂ / 0 °C

5: 1.22 g / lithium hydroxide / tetrahydrofuran; H₂O / 0 °C

6: 1.63 g / imidazole / CH₂Cl₂ / 0 °C

7: 1.55 g / 1-hydroxy-1H-benzotriazole; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide HCl; triethylamine / CH₂Cl₂ / 0 °C

With 1H-imidazole; hydrogenchloride; lithium hydroxide; sodium hydroxide; 2-phenylbenzo[d]oxazole; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1016/j.bmc.2005.08.019

Reference yield:

: 2-(2-benzyloxycarbonylamino-3-dimethylcarbamoyl-propionylamino)-2-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-pentanoic acid

: 100-46-9
benzylamine

: 872983-47-6
N-((1S)-1-{1-benzylcarbamoyl-1-[2-(tert-butyldiphenylsiloxy)ethyl]butylcarbamoyl}-3-dimethylamino-3-oxopropyl)carbamic acid benzyl 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