(S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

Base Information

Chemical Name:(S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid
CAS No.:215512-45-1
Molecular Formula:C₃₀H₃₄N₂O₆
Molecular Weight:518.61
Hs Code.:

Synonyms:(S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

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Chemical Property of (S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

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Technology Process of (S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

There total 4 articles about (S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic 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:

: 42990-55-6,35016-63-8,42990-49-8,16503-53-0
(S)-(alpha)-bromobenzenepropanoic acid

: 215512-45-1
(S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / PTS*H₂O / 2 h / Heating

2: 70 percent / NaHCO₃ / dimethylformamide

3: 85 percent / aq. NaOH

4: 98 percent / dimethylformamide / 24 h / Ambient temperature

With sodium hydroxide; PTS*H₂O; sodium hydrogencarbonate; In N,N-dimethyl-formamide;
DOI:10.1016/S0223-5234(98)80043-3

Reference yield:

: 673-06-3,25191-15-5,658-69-5,67675-33-6
D-(R)-phenylalanine

: 215512-45-1
(S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 65 percent / aq. H₂SO₄, NaNO₂, KBr / 1) 0 deg C, 2 h, 2) r.t., 2 h

2: 97 percent / PTS*H₂O / 2 h / Heating

3: 70 percent / NaHCO₃ / dimethylformamide

4: 85 percent / aq. NaOH

5: 98 percent / dimethylformamide / 24 h / Ambient temperature

With sodium hydroxide; PTS*H₂O; sulfuric acid; sodium hydrogencarbonate; potassium bromide; sodium nitrite; In N,N-dimethyl-formamide;
DOI:10.1016/S0223-5234(98)80043-3

Reference yield:

: 73136-26-2
(R)-2-bromo-3-phenylpropionic acid methyl ester

: 215512-45-1
(S)-2-[Benzyloxy-((S)-2-tert-butoxycarbonylamino-3-phenyl-propionyl)-amino]-3-phenyl-propionic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / NaHCO₃ / dimethylformamide

2: 85 percent / aq. NaOH

3: 98 percent / dimethylformamide / 24 h / Ambient temperature

With sodium hydroxide; sodium hydrogencarbonate; In N,N-dimethyl-formamide;
DOI:10.1016/S0223-5234(98)80043-3