(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Base Information

Chemical Name:(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester
CAS No.:199541-49-6
Molecular Formula:C₅₄H₆₆N₈O₁₀
Molecular Weight:987.166
Hs Code.:

(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Synonyms:(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Suppliers and Price of (S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

There total 10 articles about (S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl 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:

: 65864-22-4
(S)-2-amino-3-phenylpropionamide hydrochloride

: 199541-49-6
(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) DIEA, Piv-Cl, 2.) DIEA / 1.) DMF, 15 min, 2.) DMF, RT, 6 h

2: HCl / ethyl acetate / 1 h / -10 - 20 °C

3: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

4: HCl / ethyl acetate / 1 h / -10 - 20 °C

5: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

6: 88 percent / HCl, anisole / ethyl acetate / 1 h / -10 - 20 °C

7: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

With hydrogenchloride; pivaloyl chloride; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; methoxybenzene; N-ethyl-N,N-diisopropylamine; In ethyl acetate;
DOI:10.1021/jm970477u

Reference yield:

: 114516-71-1
(S)-methyl 2-(2-(tert-butoxycarbonylamino)hexanamido)acetate

: 199541-49-6
(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / HCl / ethyl acetate / 1 h / -10 - 20 °C

2: 77 percent / DIEA / dimethylformamide / 18 h

3: 51 percent / 1N aq. NaOH / methanol / 1 h / -10 - 20 °C

4: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

With hydrogenchloride; sodium hydroxide; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In methanol; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm970477u

Reference yield:

: 141408-45-9
(S)-4-(benzyloxy)-2-((tert-butoxycarbonyl)(methyl)amino)-4-oxobutanoic acid

: 199541-49-6
(S)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-({(S)-2-[(S)-2-(2-{(S)-2-[2-(4-hydroxy-phenyl)-acetylamino]-hexanoylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino]-hexanoyl}-methyl-amino)-succinamic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) DIEA, Piv-Cl, 2.) DIEA / 1.) DMF, 15 min, 2.) DMF, RT, 6 h

2: HCl / ethyl acetate / 1 h / -10 - 20 °C

3: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

4: HCl / ethyl acetate / 1 h / -10 - 20 °C

5: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

6: 88 percent / HCl, anisole / ethyl acetate / 1 h / -10 - 20 °C

7: 1.) TBTU, HOBt, DIEA, 2.) DIEA / 1.) DMF, 5 min, 2.) DMF, RT, 2 d

With hydrogenchloride; pivaloyl chloride; benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; methoxybenzene; N-ethyl-N,N-diisopropylamine; In ethyl acetate;
DOI:10.1021/jm970477u