(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

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Chemical Name:(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid
CAS No.:95716-15-7
Molecular Formula:C₅₂H₇₁N₇O₁₁
Molecular Weight:970.176
Hs Code.:

(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

Synonyms:(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

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Chemical Property of (S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

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Technology Process of (S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

There total 10 articles about (S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic 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: 75.0%

: 95716-13-5
(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid benzyl ester

: 95716-15-7
(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; methanol; for 12h; Ambient temperature;
DOI:10.1246/bcsj.57.3210

Reference yield:

: 13734-41-3
t-Boc-L-valine

: 95716-15-7
(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, (C₂H₅)3N / CHCl₃ / 0 deg C, 2 h; room temperature, overnight

2: HCl, anisole / dioxane / 0.5 h / Ambient temperature

3: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, (C₂H₅)3N / CHCl₃ / 0 deg C, 2 h; room temperature, overnight

4: 75 percent / 2M aq. NaOH / methanol; dioxane / 12 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; methoxybenzene; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In 1,4-dioxane; methanol; chloroform;
DOI:10.1246/bcsj.57.3210

Reference yield:

: 13139-15-6,53296-34-7
N-tert-butoxycarbonyl-L-leucine

: 95716-15-7
(S)-1-[(S)-2-((S)-5-Benzyloxycarbonylamino-2-{(S)-2-[(R)-2-((R)-2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-3-phenyl-propionylamino]-3-methyl-butyrylamino}-pentanoylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 8 steps

1: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, (C₂H₅)3N / CHCl₃ / 0 deg C, 2 h; room temperature, overnight

2: HCl, anisole / dioxane / 0.5 h / Ambient temperature

3: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, (C₂H₅)3N / CHCl₃ / 0 deg C, 2 h; room temperature, overnight

4: HCl, anisole / dioxane / 0.5 h / Ambient temperature

5: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, (C₂H₅)3N / CHCl₃ / 0 deg C, 2 h; room temperature, overnight

6: HCl, anisole / dioxane / 0.5 h / Ambient temperature

7: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, (C₂H₅)3N / CHCl₃ / 0 deg C, 2 h; room temperature, overnight

8: 75 percent / 2M aq. NaOH / methanol; dioxane / 12 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; methoxybenzene; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In 1,4-dioxane; methanol; chloroform;
DOI:10.1246/bcsj.57.3210