6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

Base Information

Chemical Name:6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide
CAS No.:428879-77-0
Molecular Formula:C₄₀H₆₅N₅O₅
Molecular Weight:695.987
Hs Code.:

Synonyms:6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

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Chemical Property of 6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

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Technology Process of 6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

There total 6 articles about 6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)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:

: 1947-00-8
6-(benzyloxycarbonylamino)hexanoic acid

: 428879-77-0
6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

1.2: 70 percent / dioxane / 20 °C

2.1: 100 percent / 30percent HBr; AcOH; CF₃COOH / 2 h

3.1: methanol / 2 h / Heating

4.1: NaBH₄ / methanol / 5 h / 20 °C

With sodium tetrahydroborate; chloroformic acid ethyl ester; acetic acid; triethylamine; trifluoroacetic acid; In 1,4-dioxane; methanol;
DOI:10.1021/jm011067f

Reference yield:

: 6-{[1-(2-Methoxy-phenyl)-meth-(Z)-ylidene]-amino}-hexanoic acid {6-[6-(6-{[1-(2-methoxy-phenyl)-meth-(Z)-ylidene]-amino}-hexanoylamino)-hexanoylamino]-hexyl}-amide

: 428879-77-0
6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 5h;
DOI:10.1021/jm011067f

Reference yield:

: 66095-18-9
N-benzyloxycarbonyl-1,6-hexanediamine

: 428879-77-0
6-(2-methoxybenzylamino)hexanoic acid (6-{6-[6-(2-methoxybenzylamino)hexanoylamino]hexanoylamino}hexyl)amide

Guidance literature:: Multi-step reaction with 6 steps

1.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

1.2: 78 percent / dioxane / 20 °C

2.1: 100 percent / H₂ / 10percent Pd/C / methanol / 2 h

3.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

3.2: 70 percent / dioxane / 20 °C

4.1: 100 percent / 30percent HBr; AcOH; CF₃COOH / 2 h

5.1: methanol / 2 h / Heating

6.1: NaBH₄ / methanol / 5 h / 20 °C

With sodium tetrahydroborate; hydrogen; chloroformic acid ethyl ester; acetic acid; triethylamine; trifluoroacetic acid; 10percent Pd/C; In 1,4-dioxane; methanol;
DOI:10.1021/jm011067f