N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

Base Information

Chemical Name:N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide
CAS No.:1300031-03-1
Molecular Formula:C₂₃H₂₀ClN₃O₂
Molecular Weight:405.884
Hs Code.:

Synonyms:N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

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Technology Process of N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

There total 3 articles about N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide 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: 24.0%

: 262862-71-5
(4-(4-chlorophenoxy)phenyl)methanamine hydrochloride

: 81438-53-1
2,7-dimethylimidazo[1,2-a]pyridine-3-carboxylic acid

: 1300031-03-1
N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In acetonitrile; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1021/ml400088y

Reference yield:

: 695-34-1
2-Amino-4-methylpyridine

: 1300031-03-1
N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1,2-dimethoxyethane / 48 h / Reflux; Inert atmosphere

2: lithium hydroxide / ethanol / Inert atmosphere

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / acetonitrile / 12 h / 20 °C / Inert atmosphere

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In 1,2-dimethoxyethane; ethanol; acetonitrile;
DOI:10.1021/ml400088y

Reference yield:

: 81448-48-8
ethyl 2,7-dimethylimidazo[1,2-a]pyridine-3-carboxylate

: 1300031-03-1
N-(4-(4-Chlorophenoxy)benzyl)-2,7-dimethylimidazo[1,2-a]pyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide / ethanol / Inert atmosphere

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / acetonitrile / 12 h / 20 °C / Inert atmosphere

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; lithium hydroxide; In ethanol; acetonitrile;
DOI:10.1021/ml400088y