7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

Base Information

Chemical Name:7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide
CAS No.:135429-07-1
Molecular Formula:C₁₆H₁₄Cl₂N₄O
Molecular Weight:349.219
Hs Code.:

Synonyms:7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

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Chemical Property of 7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

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Technology Process of 7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

There total 9 articles about 7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide 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: 18.0%

: 118698-09-2
2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide 4-oxide

: 135429-07-1
7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

Guidance literature:: With trichlorophosphate; Heating;
DOI:10.1021/jm00114a007

Reference yield:

: 5470-18-8,34515-82-7
2-Chloro-3-nitropyridine

: 135429-07-1
7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

Guidance literature:: Multi-step reaction with 8 steps

1: 90 percent / Et₃N / ethanol / 1.75 h / Heating

2: H₂ / 5percent Pd/C / tetrahydrofuran / 1 h / Ambient temperature

3: 87 percent / Et₃N / tetrahydrofuran / Ambient temperature

4: 48 percent / 0.13 h / 210 - 220 °C

5: 58 percent / aq. NaOH / ethanol / 0.75 h / Heating

6: 1.) 1,1'-carbonyldiimidazole / 1.) THF, RT, 3 h, 2.) THF, RT, overnight

7: 88 percent / m-chloroperbenzoic acid, AcOH / 4 h / 60 °C

8: 18 percent / POCl₃ / Heating

With sodium hydroxide; hydrogen; acetic acid; triethylamine; 3-chloro-benzenecarboperoxoic acid; 1,1'-carbonyldiimidazole; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00114a007

Reference yield:

: 90559-63-0
N-(3-nitro-2-pyridinyl)glycine ethyl ester

: 135429-07-1
7-chloro-2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo<4,5-b>pyridine-3-acetamide

Guidance literature:: Multi-step reaction with 7 steps

1: H₂ / 5percent Pd/C / tetrahydrofuran / 1 h / Ambient temperature

2: 87 percent / Et₃N / tetrahydrofuran / Ambient temperature

3: 48 percent / 0.13 h / 210 - 220 °C

4: 58 percent / aq. NaOH / ethanol / 0.75 h / Heating

5: 1.) 1,1'-carbonyldiimidazole / 1.) THF, RT, 3 h, 2.) THF, RT, overnight

6: 88 percent / m-chloroperbenzoic acid, AcOH / 4 h / 60 °C

7: 18 percent / POCl₃ / Heating

With sodium hydroxide; hydrogen; acetic acid; triethylamine; 3-chloro-benzenecarboperoxoic acid; 1,1'-carbonyldiimidazole; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00114a007