N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide

Base Information

• Chemical Name: N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide
• CAS No.: 133728-32-2
• Molecular Formula: C₁₉H₂₆ClN₃O₂Si
• Molecular Weight: 391.973
• Mol file: 133728-32-2.mol

Synonyms:N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide

Chemical Property of N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide

There total 3 articles about N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide 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: 36.0%

2-chloro-3-aminopyridine (6298-19-7) + methyl 2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzoate (133727-56-7) → N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide (133728-32-2)

Guidance literature:

With potassium tert-butylate; In tetrahydrofuran; for 2h;

DOI:10.1021/jm00111a032

Reference yield:

dimethyl aminoterephthalate (5372-81-6) → N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide (133728-32-2)

Guidance literature:

Multi-step reaction with 3 steps

1: super-hydride 3)H> / tetrahydrofuran / -78 °C

2: tetrahydrofuran

3: 36 percent / potassium tert-butoxide / tetrahydrofuran / 2 h

With potassium tert-butylate; lithium triethylborohydride; In tetrahydrofuran;

DOI:10.1021/jm00111a032

Reference yield:

methyl 2-amino-4-(hydroxymethyl)benzoate (133728-31-1) → N-(2'-chloro-3-pyridyl)-2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzamide (133728-32-2)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrahydrofuran

2: 36 percent / potassium tert-butoxide / tetrahydrofuran / 2 h

With potassium tert-butylate; In tetrahydrofuran;

DOI:10.1021/jm00111a032

upstream raw materials:

2-chloro-3-aminopyridine

methyl 2-amino-4-<<(dimethyl-tert-butylsilyl)oxy>methyl>benzoate

dimethyl aminoterephthalate

methyl 2-amino-4-(hydroxymethyl)benzoate