(3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

Base Information

Chemical Name:(3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide
CAS No.:1381873-11-5
Molecular Formula:C₂₆H₃₈N₂O₃
Molecular Weight:426.599
Hs Code.:

Synonyms:(3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

Chemical Property:

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Technology Process of (3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

There total 6 articles about (3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide 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:

: C₂HF₃O₂*C₂₆H₃₈N₂O₃

: 1381873-11-5
(3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/j.tetlet.2012.04.018

Reference yield:

: 72155-45-4
Boc-L-phenylalaninal

: 1381873-11-5
(3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane / 72 h / 20 °C

2: dichloromethane / 2 h / 20 °C

3: triethylamine / dichloromethane / 1 h / 20 °C

With triethylamine; In dichloromethane; 1: Passerini reaction;
DOI:10.1016/j.tetlet.2012.04.018

Reference yield:

: 87694-53-9
Boc-Phe-OH N,O-dimethyl hydroxamate

: 1381873-11-5
(3S)-N-(adamantan-1-yl)-3-(3,3-dimethylbutanamido)-2-hydroxy-4-phenylbutanamide

Guidance literature:: Multi-step reaction with 4 steps

1: lithium aluminium tetrahydride

2: dichloromethane / 72 h / 20 °C

3: dichloromethane / 2 h / 20 °C

4: triethylamine / dichloromethane / 1 h / 20 °C

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