3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

Base Information

Chemical Name:3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile
CAS No.:213315-41-4
Molecular Formula:C₂₂H₂₃N₃O₂S
Molecular Weight:393.51
Hs Code.:

Synonyms:3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

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Chemical Property of 3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

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Technology Process of 3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

There total 5 articles about 3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile 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: 39.0%

: 213315-36-7
methyl 3-(3-chloropropylamino)propionitrile

: 213315-40-3
4-(4-thiazol-2-ylphenoxy)phenol

: 213315-41-4
3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

Guidance literature:: 4-(4-thiazol-2-ylphenoxy)phenol; With potassium hydroxide; In dimethyl sulfoxide; at 20 ℃; for 0.0833333h;

methyl 3-(3-chloropropylamino)propionitrile; In dimethyl sulfoxide; at 45 ℃; for 4h; Further stages.;
DOI:10.1021/jm0200916

Reference yield:

: 78338-68-8
4-(4-methoxyphenoxy)benzonitrile

: 213315-41-4
3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: 89 percent / KOH / 2-methyl-propan-2-ol; dimethylsulfoxide / 2 h / Heating

2.1: 49 percent / Lawesson's reagent / toluene / 3 h / Heating

3.1: oxalic acid / 1 h / Heating

3.2: 2 h / Heating

3.3: 50 percent / 30percent aq. HCl / 0.5 h / Heating

4.1: 78 percent / boron tribromide / CH₂Cl₂ / 3 h / -78 - 20 °C

5.1: KOH / dimethylsulfoxide / 0.08 h / 20 °C

5.2: 39 percent / dimethylsulfoxide / 4 h / 45 °C

With Lawessons reagent; potassium hydroxide; oxalic acid; boron tribromide; In dichloromethane; dimethyl sulfoxide; toluene; tert-butyl alcohol;
DOI:10.1021/jm0200916

Reference yield:

: 213315-38-9
4-(4-methoxyphenoxy)thiobenzamide

: 213315-41-4
3-(methyl-[3-[4-(4-thiazol-2-ylphenoxy)phenoxy]propyl]amino)propionitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: oxalic acid / 1 h / Heating

1.2: 2 h / Heating

1.3: 50 percent / 30percent aq. HCl / 0.5 h / Heating

2.1: 78 percent / boron tribromide / CH₂Cl₂ / 3 h / -78 - 20 °C

3.1: KOH / dimethylsulfoxide / 0.08 h / 20 °C

3.2: 39 percent / dimethylsulfoxide / 4 h / 45 °C

With potassium hydroxide; oxalic acid; boron tribromide; In dichloromethane; dimethyl sulfoxide;
DOI:10.1021/jm0200916