(S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

Base Information

Chemical Name:(S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide
CAS No.:1027841-46-8
Molecular Formula:C₂₂H₃₀N₄O₃
Molecular Weight:398.505
Hs Code.:

Synonyms:(S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

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Chemical Property of (S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

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Technology Process of (S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

There total 4 articles about (S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide 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: 89.0%

: 253344-35-3
{1-[3-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-1-hydroxymethyl-propylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester

: 1027841-46-8
(S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

Guidance literature:: With trifluoroacetic acid; In methoxybenzene;
DOI:10.1016/S0223-5234(00)80034-3

Reference yield:

: 3674-06-4
Boc-Phe-ONSu

: 1027841-46-8
(S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 4 steps

1: N-methylmorpholine / dimethylformamide / 8 h / 20 °C

2: N-methylmorpholine / tetrahydrofuran / 0.33 h / -15 °C

3: NaBH₄ / tetrahydrofuran; ethanol / 0.42 h / 0 - 20 °C

4: 89 percent / aq. TFA / methoxybenzene

With 4-methyl-morpholine; sodium tetrahydroborate; trifluoroacetic acid; In tetrahydrofuran; ethanol; methoxybenzene; N,N-dimethyl-formamide; 1: Substitution / 2: Substitution / 3: Reduction / 4: Hydrolysis;
DOI:10.1016/S0223-5234(00)80034-3

Reference yield:

: C₃₇H₅₂N₄O₁₀

: 1027841-46-8
(S)-2-Amino-N-[(S)-3-((S)-2-amino-3-phenyl-propionylamino)-1-hydroxymethyl-propyl]-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄ / tetrahydrofuran; ethanol / 0.42 h / 0 - 20 °C

2: 89 percent / aq. TFA / methoxybenzene

With sodium tetrahydroborate; trifluoroacetic acid; In tetrahydrofuran; ethanol; methoxybenzene; 1: Reduction / 2: Hydrolysis;
DOI:10.1016/S0223-5234(00)80034-3