(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Base Information

Chemical Name:(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane
CAS No.:143348-09-8
Molecular Formula:C₄₂H₅₆N₆O₈
Molecular Weight:772.942
Hs Code.:

(2S,3S)-3-<<N-(benzyloxycarbonyl)asparaginyl>amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Synonyms:(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Suppliers and Price of (2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

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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 (2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Chemical Property:

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Technology Process of (2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

There total 6 articles about (2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane 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:

: 132234-38-9,137253-05-5,143395-66-8
(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalanine methyl ester)butane

: 143348-09-8
(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Guidance literature:: With sodium tetrahydroborate; In methanol; at 0 ℃; for 6h;
DOI:10.1021/jm00099a008

Reference yield:

: 2304-96-3
N-benzyloxycarbonyl-L-asparagine

: 143348-09-8
(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) hydroxybenzotriazole (HOBt), EDCI, 2.) N-methylmorpholine (NMM) / 1.) DMF, 40 min, 2.) DMF, a) 0 deg C, 2 h, b) RT, overnight

2: NaBH₄ / methanol / 6 h / 0 °C

With 4-methyl-morpholine; sodium tetrahydroborate; benzotriazol-1-ol; In methanol;
DOI:10.1021/jm00099a008

Reference yield:

: 103127-52-2,107202-43-7
((S)-1-benzylallyl)carbamic acid tert-butyl ester

: 143348-09-8
(2S,3S)-3-<amino>-2-hydroxy-4-phenyl-1-(N-prolylisoleucinylphenylalaninol)butane

Guidance literature:: Multi-step reaction with 5 steps

1: mCPBA / CH₂Cl₂ / 0 °C

2: triethylamine / diisopropyl ether / 24 h / Heating

3: 4 N HCl / dioxane / 1 h / Ambient temperature

4: 1.) hydroxybenzotriazole (HOBt), EDCI, 2.) N-methylmorpholine (NMM) / 1.) DMF, 40 min, 2.) DMF, a) 0 deg C, 2 h, b) RT, overnight

5: NaBH₄ / methanol / 6 h / 0 °C

With 4-methyl-morpholine; hydrogenchloride; sodium tetrahydroborate; benzotriazol-1-ol; triethylamine; 3-chloro-benzenecarboperoxoic acid; In 1,4-dioxane; methanol; dichloromethane; di-isopropyl ether;
DOI:10.1021/jm00099a008