N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

Base Information

Chemical Name:N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine
CAS No.:1620482-49-6
Molecular Formula:C₂₈H₂₈N₈O
Molecular Weight:492.583
Hs Code.:

Synonyms:N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

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Chemical Property of N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

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Technology Process of N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

There total 3 articles about N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine 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: 68.0%

: 500-22-1
3-pyridinecarboxaldehyde

: 88333-03-3,10340-91-7
Benzyl isocyanide

: 1620483-13-7
N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

: 1620482-49-6
N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

Guidance literature:: With trimethylsilylazide; In methanol; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja505517t

Reference yield:

: 1620483-11-5
{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]phenyl}methanol

: 1620482-49-6
N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

Guidance literature:: Multi-step reaction with 3 steps

1: sulfur trioxide pyridine complex; triethylamine / ethyl acetate; dimethyl sulfoxide / 0.33 h / 0 - 20 °C / Inert atmosphere

2: sodium tris(acetoxy)borohydride / acetonitrile; dichloromethane / 15 h / 0 - 20 °C / Inert atmosphere

3: trimethylsilylazide / methanol / 0 - 20 °C / Inert atmosphere

With trimethylsilylazide; sulfur trioxide pyridine complex; sodium tris(acetoxy)borohydride; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; acetonitrile;
DOI:10.1021/ja505517t

Reference yield:

: 1620483-12-6
4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzaldehyde

: 1620482-49-6
N-[(1-benzyl-1H-tetrazol-5-yl)(3-pyridinyl)methyl]-N-{4-[2-(3-methyl-3H-diaziren-3-yl)ethoxy]benzyl}-2-propyn-1-amine

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tris(acetoxy)borohydride / acetonitrile; dichloromethane / 15 h / 0 - 20 °C / Inert atmosphere

2: trimethylsilylazide / methanol / 0 - 20 °C / Inert atmosphere

With trimethylsilylazide; sodium tris(acetoxy)borohydride; In methanol; dichloromethane; acetonitrile;
DOI:10.1021/ja505517t