(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

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Chemical Name:(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid
CAS No.:406712-32-1
Molecular Formula:C₄₁H₆₄N₈O₁₂S
Molecular Weight:893.072
Hs Code.:

(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

Synonyms:(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

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Chemical Property of (S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

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Technology Process of (S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

There total 1 articles about (S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-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: 95.0%

: 3392-09-4
Boc-Leu-ONSu

: (S)-2-({(S)-1-[(S)-2-[(R)-3-(Acetylamino-methylsulfanyl)-2-((S)-2-amino-3-methyl-butyrylamino)-propionylamino]-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid; compound with trifluoro-acetic acid

: 406712-32-1
(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1023/A:1012901200640

Reference yield: 94.3%

: 76-05-1
trifluoroacetic acid

: 406712-32-1
(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

: (S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-amino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid; compound with trifluoro-acetic acid

Guidance literature:: at 20 ℃; for 1h;
DOI:10.1023/A:1012901200640

Reference yield:

: 406712-32-1
(S)-2-({(S)-1-[(S)-2-{(R)-3-(Acetylamino-methylsulfanyl)-2-[(S)-2-((S)-2-tert-butoxycarbonylamino-4-methyl-pentanoylamino)-3-methyl-butyrylamino]-propionylamino}-3-(4-hydroxy-phenyl)-propionyl]-pyrrolidine-2-carbonyl}-amino)-4-carbamoyl-butyric acid

: 193750-09-3
H-Leu-Val-Cys-Tyr-Pro-Gln-OH

Guidance literature:: Multi-step reaction with 2 steps

1: 94.3 percent / 1 h / 20 °C

2: 51 percent / Hg(OAc)2 / acetic acid; H₂O / 1.5 h / 20 °C

With mercury(II) diacetate; In water; acetic acid;
DOI:10.1023/A:1012901200640