7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

Base Information

Chemical Name:7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester
CAS No.:1036742-51-4
Molecular Formula:C₂₁H₃₂N₆O₃
Molecular Weight:416.523
Hs Code.:

Synonyms:7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

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Chemical Property of 7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

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Technology Process of 7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

There total 5 articles about 7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic 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: 91.0%

: 88192-19-2
3-azidopropylamine

: 1036742-50-3
7-(4-prop-2-ynylamino-benzoylamino)-heptanoic acid methyl ester

: 1036742-51-4
7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

Guidance literature:: With tetrakis(acetonitrile)copper(I)hexafluorophosphate; tris-(1-benzyl-1H-1,2,3-triazol-4-ylmethyl)amine; In acetonitrile; at 60 ℃; for 16h;
DOI:10.1016/j.bmcl.2008.04.007

Reference yield:

: 17994-94-4
methyl 7-aminoheptanoate hydrochloride

: 1036742-51-4
7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 4-methyl-morpholine; isobutyl chloroformate / tetrahydrofuran / 0.25 h / 0 °C / Inert atmosphere

1.2: 3 h / 0 - 20 °C / Inert atmosphere

2.1: palladium 10% on activated carbon; hydrogen / methanol / 2.5 h / 20 °C / Inert atmosphere

3.1: potassium carbonate / N,N-dimethyl-formamide; toluene / 50 °C / Inert atmosphere

4.1: tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; tetrakis(actonitrile)copper(I) hexafluorophosphate / acetonitrile / 16 h / 60 °C / Inert atmosphere

With 4-methyl-morpholine; tetrakis(actonitrile)copper(I) hexafluorophosphate; palladium 10% on activated carbon; hydrogen; potassium carbonate; isobutyl chloroformate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1021/acsmedchemlett.9b00471

Reference yield:

: 1036742-52-5
7-(4-nitrobenzoylamino)-heptanoic acid methyl ester

: 1036742-51-4
7-(4-((1-((3-aminopropyl)-1H-1,2,3-triazol-4-yl)methyl)amino)benzamido)heptanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 2.5 h / 20 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide; toluene / 50 °C / Inert atmosphere

3: tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; tetrakis(actonitrile)copper(I) hexafluorophosphate / acetonitrile / 16 h / 60 °C / Inert atmosphere

With tetrakis(actonitrile)copper(I) hexafluorophosphate; palladium 10% on activated carbon; hydrogen; potassium carbonate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In methanol; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1021/acsmedchemlett.9b00471