(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Base Information

Chemical Name:(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester
CAS No.:393547-03-0
Molecular Formula:C₅₀H₇₆N₈O₁₃
Molecular Weight:997.199
Hs Code.:

(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Synonyms:(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

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Chemical Property of (S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

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Technology Process of (S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

There total 9 articles about (S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl 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:

: 100-39-0
benzyl bromide

: 393547-03-0
(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 10 steps

1.1: K₂CO₃; TBAI / 1,2-dimethoxy-ethane

2.1: HBr; AcOH

3.1: KO-tBu / tetrahydrofuran / -40 °C

3.2: tetrahydrofuran / -40 °C

4.1: 100 percent / H₂ / Pd/C / ethanol

5.1: 91 percent / EDCI; HOBt; NMM

6.1: HCl / dioxane

7.1: EDCI; HOBt; NMM

8.1: 78 percent / Dess-Martin periodinane

9.1: HCl / dioxane

10.1: EDCI; HOBt; NMM

With 4-methyl-morpholine; hydrogenchloride; potassium tert-butylate; hydrogen bromide; hydrogen; tetra-(n-butyl)ammonium iodide; potassium carbonate; benzotriazol-1-ol; Dess-Martin periodane; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; ethanol;
DOI:10.1016/j.bmcl.2004.09.058

Reference yield:

: 89371-46-0
benzyl (4S)-1-benzyl-2-oxoimidazolidine-4-carboxylate

: 393547-03-0
(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: KO-tBu / tetrahydrofuran / -40 °C

1.2: tetrahydrofuran / -40 °C

2.1: 100 percent / H₂ / Pd/C / ethanol

3.1: 91 percent / EDCI; HOBt; NMM

4.1: HCl / dioxane

5.1: EDCI; HOBt; NMM

6.1: 78 percent / Dess-Martin periodinane

7.1: HCl / dioxane

8.1: EDCI; HOBt; NMM

With 4-methyl-morpholine; hydrogenchloride; potassium tert-butylate; hydrogen; benzotriazol-1-ol; Dess-Martin periodane; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1016/j.bmcl.2004.09.058

Reference yield:

: 89371-88-0
benzyl (4S)-1-benzyl-3-benzyloxycarbonyl-2-oxo-imidazolidine-4-carboxylate

: 393547-03-0
(S)-4-((S)-2-Acetylamino-4-tert-butoxycarbonyl-butyrylamino)-4-((S)-1-{(S)-1-[(S)-5-(1-allylaminooxalyl-butylcarbamoyl)-3-benzyl-2-oxo-imidazolidine-1-carbonyl]-2-methyl-propylcarbamoyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1.1: HBr; AcOH

2.1: KO-tBu / tetrahydrofuran / -40 °C

2.2: tetrahydrofuran / -40 °C

3.1: 100 percent / H₂ / Pd/C / ethanol

4.1: 91 percent / EDCI; HOBt; NMM

5.1: HCl / dioxane

6.1: EDCI; HOBt; NMM

7.1: 78 percent / Dess-Martin periodinane

8.1: HCl / dioxane

9.1: EDCI; HOBt; NMM

With 4-methyl-morpholine; hydrogenchloride; potassium tert-butylate; hydrogen bromide; hydrogen; benzotriazol-1-ol; Dess-Martin periodane; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1016/j.bmcl.2004.09.058