(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

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Chemical Name:(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}
CAS No.:145484-73-7
Molecular Formula:C₃₈H₅₄N₁₀O₇S
Molecular Weight:794.976
Hs Code.:

(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

Synonyms:(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

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Chemical Property of (S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

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Technology Process of (S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

There total 1 articles about (S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide} 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:

: 145484-59-9
{(S)-3-Carbamoyl-1-[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethylcarbamoyl]-propyl}-carbamic acid tert-butyl ester

: 145484-73-7
(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; for 0.75h;
DOI:10.1021/jm00053a001

Reference yield:

: 145484-73-7
(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

: (S)-2-[(S)-2-(2-{(S)-2-[(S)-2-((S)-2-Amino-4-carbamoyl-butyrylamino)-3-(1H-indol-3-yl)-propionylamino]-3-phenyl-propionylamino}-acetylamino)-4-methyl-pentanoylamino]-4-methylsulfanyl-butyryl azide; hydrochloride

Guidance literature:: With hydrogenchloride; isopentyl nitrite; In tetrahydrofuran; N,N-dimethyl-formamide; at -25 ℃; for 2h; Yield given;
DOI:10.1021/jm00053a001

Reference yield:

: 145484-73-7
(S)-2-Amino-pentanedioic acid 5-amide 1-{[(S)-1-[(S)-1-({[(S)-1-((S)-1-hydrazinocarbonyl-3-methylsulfanyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-methyl}-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-(1H-indol-3-yl)-ethyl]-amide}

: cyclo-(Met-Gln-Trp-Phe-Gly-Leu)

Guidance literature:: Multi-step reaction with 2 steps

1: HCl, isopentylnitrite / dimethylformamide; tetrahydrofuran / 2 h / -25 °C

2: 678 mg / Et₃N / dimethylformamide / 20 h / -25 °C

With hydrogenchloride; triethylamine; isopentyl nitrite; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jm00053a001