(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

Base Information

Chemical Name:(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid
CAS No.:871805-44-6
Molecular Formula:C₃₂H₅₁N₅O₉
Molecular Weight:649.785
Hs Code.:

Synonyms:(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

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Chemical Property of (S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

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Technology Process of (S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

There total 2 articles about (S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid 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:

: 871102-98-6
3,5-bis-(2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoic acid

: 871805-44-6
(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / dicyclohexylcarbodiimide; 4-methylmorpholine; 1H-benzotriazol-1-ol / tetrahydrofuran / 22 h / -10 - 25 °C

2: 94 percent / KOH / H₂O; methanol / 25 °C

With 4-methyl-morpholine; potassium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; water;
DOI:10.1016/j.tet.2005.08.006

Reference yield:

: 6306-52-1
L-valine methylester hydrochloride

: 871805-44-6
(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / dicyclohexylcarbodiimide; 4-methylmorpholine; 1H-benzotriazol-1-ol / tetrahydrofuran / 22 h / -10 - 25 °C

2: 94 percent / KOH / H₂O; methanol / 25 °C

With 4-methyl-morpholine; potassium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; water;
DOI:10.1016/j.tet.2005.08.006

Reference yield: 46.0%

: 871805-44-6
(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyric acid

: 871805-48-0
3-Amino-5-{(S)-2-[3,5-bis-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-benzoylamino]-3-phenyl-propionylamino}-benzoic acid ethyl ester

: 3-{(S)-2-[3,5-Bis-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-benzoylamino]-3-methyl-butyrylamino}-5-{(S)-2-[3,5-bis-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-benzoylamino]-3-phenyl-propionylamino}-benzoic acid ethyl ester

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; at -10 - 25 ℃; for 50h;
DOI:10.1016/j.tet.2005.08.006