(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

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Chemical Name:(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester
CAS No.:1026943-13-4
Molecular Formula:C₃₅H₅₇N₃O₁₃S₄
Molecular Weight:856.114
Hs Code.:

(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

Synonyms:(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

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Chemical Property of (3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

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Technology Process of (3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

There total 5 articles about (3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl 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:

: 35444-44-1
methyl adipoyl chloride

: 1026943-13-4
(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / Et₃N / dimethylformamide / 7 h / 0 - 20 °C

2: 92 percent / 0.1 N aq. NaOH / 7 h / Ambient temperature

3: dicyclohexylcarbodiimide, 1-hydroxybenzotriazole / ethyl acetate; acetone / 24 h / Ambient temperature

With sodium hydroxide; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In ethyl acetate; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm00053a016

Reference yield:

: 138-37-4
mafenide hydrochloride

: 1026943-13-4
(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / Et₃N / dimethylformamide / 7 h / 0 - 20 °C

2: 92 percent / 0.1 N aq. NaOH / 7 h / Ambient temperature

3: dicyclohexylcarbodiimide, 1-hydroxybenzotriazole / ethyl acetate; acetone / 24 h / Ambient temperature

With sodium hydroxide; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In ethyl acetate; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm00053a016

Reference yield:

: 928211-28-3
5-(4-Sulfamoyl-benzylcarbamoyl)-pentanoic acid methyl ester

: 1026943-13-4
(3-{3-(3-Methoxycarbonylmethylsulfanyl-propoxy)-2-(3-methoxycarbonylmethylsulfanyl-propoxymethyl)-2-[5-(4-sulfamoyl-benzylcarbamoyl)-pentanoylamino]-propoxy}-propylsulfanyl)-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / 0.1 N aq. NaOH / 7 h / Ambient temperature

2: dicyclohexylcarbodiimide, 1-hydroxybenzotriazole / ethyl acetate; acetone / 24 h / Ambient temperature

With sodium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In ethyl acetate; acetone;
DOI:10.1021/jm00053a016