4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine

Base Information

• Chemical Name: 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine
• CAS No.: 1187836-78-7
• Molecular Formula: C₂₃H₂₅N₇OS₂
• Molecular Weight: 479.63
• Mol file: 1187836-78-7.mol

Synonyms:4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine

Chemical Property of 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine

There total 6 articles about 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-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: 58.0%

3-phenyl-propionaldehyde (104-53-0) + 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-1,3-thiazol-2-amine (1187837-01-9) → 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine (1187836-78-7)

Guidance literature:

3-phenyl-propionaldehyde; 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-1,3-thiazol-2-amine; With sodium tris(acetoxy)borohydride; acetic acid; In 1,2-dichloro-ethane; at 20 ℃; for 38h; Inert atmosphere;

With sodium hydrogencarbonate; In dichloromethane; water; 1,2-dichloro-ethane;

Reference yield:

N-methoxy-N-methyl-3-(methylsulfanyl)benzamide (616196-32-8) → 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine (1187836-78-7)

Guidance literature:

Multi-step reaction with 4 steps

1.1: isopropylmagnesium chloride / tetrahydrofuran / 0 °C

1.2: 5 - 20 °C

2.1: pyridine; hydroxylamine hydrochloride / 5 h / 70 °C

3.1: caesium carbonate / potassium iodide / acetonitrile / 26 h / 20 °C

4.1: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / 38 h / 20 °C / Inert atmosphere

With pyridine; hydroxylamine hydrochloride; isopropylmagnesium chloride; sodium tris(acetoxy)borohydride; caesium carbonate; acetic acid; potassium iodide; In tetrahydrofuran; 1,2-dichloro-ethane; acetonitrile;

Reference yield:

N-hydroxy-1-[3-(methylsulfanyl)phenyl]-1-(1-methyl-1H-tetrazol-5-yl)methanimine (1187836-98-1) → 4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-N-(3-phenylpropyl)-1,3-thiazol-2-amine (1187836-78-7)

Guidance literature:

Multi-step reaction with 2 steps

1: caesium carbonate / potassium iodide / acetonitrile / 26 h / 20 °C

2: sodium tris(acetoxy)borohydride; acetic acid / 1,2-dichloro-ethane / 38 h / 20 °C / Inert atmosphere

With sodium tris(acetoxy)borohydride; caesium carbonate; acetic acid; potassium iodide; In 1,2-dichloro-ethane; acetonitrile;

upstream raw materials:

3-phenyl-propionaldehyde

4-{[({[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methylene}amino)oxy]methyl}-1,3-thiazol-2-amine

N-methoxy-N-methyl-3-(methylsulfanyl)benzamide

[3-(methylsulfanyl)phenyl](1-methyl-1H-tetrazol-5-yl)methanone