5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

Base Information

Chemical Name:5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine
CAS No.:1201688-26-7
Molecular Formula:C₁₉H₁₈N₄S
Molecular Weight:334.445
Hs Code.:

Synonyms:5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

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Chemical Property of 5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

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Technology Process of 5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

There total 4 articles about 5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine 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:

: 25433-14-1
1-methyl-4-phenyl-1,3-dihydroimidazole-2-thione

: C₉H₆ClF₃N₂

: 1201688-26-7
5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 60 ℃; for 2h;

Reference yield:

: 34486-24-3
2-amino-6-(trifluoromethyl)pyridine

: 1201688-26-7
5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1,2-dimethoxyethane / 20 °C

1.2: 2 h / Reflux

2.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 60 °C

With N-ethyl-N,N-diisopropylamine; In 1,2-dimethoxyethane; N,N-dimethyl-formamide;

Reference yield:

: 23826-47-3
2-(methylamino)-1-phenylethanone hydrochloride

: 1201688-26-7
5-methyl-2-(1-methyl-4-phenyl-1H-imidazol-2-ylsulfanylmethyl)-imidazo[1,2-a]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / 0.17 h / 140 °C / Microwave irradiation

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 60 °C

With acetic acid; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;