(S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

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Chemical Name:(S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester
CAS No.:189573-57-7
Molecular Formula:C₂₄H₃₇N₅O₅
Molecular Weight:475.588
Hs Code.:

Synonyms:(S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

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Chemical Property of (S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

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Technology Process of (S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

There total 5 articles about (S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester 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:

: 33300-72-0
N-tert-butoxycarbonyl-L-alanyl-L-proline

: 189573-57-7
(S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 86 percent / NMM, HOBT, EDCI / dimethylformamide / 24 h / -15 - 20 °C

2: 100 percent / HCl / dioxane / 3 h

3: 86 percent / NMM, HOBT, EDCI / dimethylformamide / 24 h / -15 - 20 °C

4: 1) Me₃SiI, 2) MeOH / 1) CH₃CN, room temperature, 10 min 2) CH₃CN

With 4-methyl-morpholine; hydrogenchloride; methanol; trimethylsilyl iodide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/ja963269k

Reference yield:

: 33300-71-9
(S)-methyl 1-((S)-2-((tert-butoxycarbonyl)amino)propanoyl)pyrrolidine-2-carboxylate

: 189573-57-7
(S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: aq. NaOH / ethanol / 6 h / Ambient temperature

2: 86 percent / NMM, HOBT, EDCI / dimethylformamide / 24 h / -15 - 20 °C

3: 100 percent / HCl / dioxane / 3 h

4: 86 percent / NMM, HOBT, EDCI / dimethylformamide / 24 h / -15 - 20 °C

5: 1) Me₃SiI, 2) MeOH / 1) CH₃CN, room temperature, 10 min 2) CH₃CN

With 4-methyl-morpholine; hydrogenchloride; methanol; sodium hydroxide; trimethylsilyl iodide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/ja963269k

Reference yield:

: 189573-54-4
(S)-2-{[(S)-1-((S)-2-tert-Butoxycarbonylamino-propionyl)-pyrrolidine-2-carbonyl]-amino}-propionic acid ethyl ester

: 189573-57-7
(S)-2-[((S)-1-{(S)-2-[(S)-2-Amino-3-(4-dimethylamino-phenyl)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / HCl / dioxane / 3 h

2: 86 percent / NMM, HOBT, EDCI / dimethylformamide / 24 h / -15 - 20 °C

3: 1) Me₃SiI, 2) MeOH / 1) CH₃CN, room temperature, 10 min 2) CH₃CN

With 4-methyl-morpholine; hydrogenchloride; methanol; trimethylsilyl iodide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/ja963269k