(3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

Base Information

Chemical Name:(3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate
CAS No.:1381872-79-2
Molecular Formula:C₃₁H₄₆N₂O₅
Molecular Weight:526.717
Hs Code.:

Synonyms:(3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

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Chemical Property of (3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

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Technology Process of (3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

There total 4 articles about (3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate 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: 42.0%

: 1070-83-3
tert-Butylacetic acid

: 22110-53-8
1-adamantyl isocyanide

: 72155-45-4
Boc-L-phenylalaninal

: 1381872-79-2
(3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

Guidance literature:: In dichloromethane; at 20 ℃; for 72h;
DOI:10.1016/j.tetlet.2012.04.018

Reference yield:

: 768-94-5
1-Adamantanamine

: 1381872-79-2
(3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

Guidance literature:: Multi-step reaction with 3 steps

1: acetic anhydride

2: triethylamine; trichlorophosphate / dichloromethane

3: dichloromethane / 72 h / 20 °C

With acetic anhydride; triethylamine; trichlorophosphate; In dichloromethane; 3: Passerini reaction;
DOI:10.1016/j.tetlet.2012.04.018

Reference yield:

: 3405-48-9
N-(1-adamantyl)formamide

: 1381872-79-2
(3S)-1-(adamantan-1-ylamino)-3-[(tert-butoxycarbonyl)amino]-1-oxo-4-phenylbutan-2-yl 3,3-dimethylbutanoate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; trichlorophosphate / dichloromethane

2: dichloromethane / 72 h / 20 °C

With triethylamine; trichlorophosphate; In dichloromethane; 2: Passerini reaction;
DOI:10.1016/j.tetlet.2012.04.018