6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

Base Information

Chemical Name:6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione
CAS No.:1423599-75-0
Molecular Formula:C₂₄H₁₉FN₄S
Molecular Weight:414.506
Hs Code.:

Synonyms:6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

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Chemical Property of 6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

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Technology Process of 6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

There total 4 articles about 6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione 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: 60.0%

: 1423600-04-7
1-(4-fluorophenyl)-3-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)prop-2-en-1-one

: 17356-08-0
thiourea

: 1423599-75-0
6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

Guidance literature:: With sodium hydroxide; In ethanol; at 80 ℃; for 6h;
DOI:10.1016/j.bmcl.2012.12.035

Reference yield:

: 1603-40-3
3-methylpyridin-2-ylamine

: 1423599-75-0
6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / 6 h / Reflux

2: trichlorophosphate / 6 h / 80 °C

3: sodium hydroxide / ethanol; water / 4 h / 50 °C

4: sodium hydroxide / ethanol / 6 h / 80 °C

With sodium hydroxide; trichlorophosphate; In ethanol; water;
DOI:10.1016/j.bmcl.2012.12.035

Reference yield:

: 70-11-1
α-bromoacetophenone

: 1423599-75-0
6-(4-fluorophenyl)-4-(8-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)-3,4-dihydropyrimidine-2(1H)-thione

Guidance literature:: Multi-step reaction with 4 steps

1: ethanol / 6 h / Reflux

2: trichlorophosphate / 6 h / 80 °C

3: sodium hydroxide / ethanol; water / 4 h / 50 °C

4: sodium hydroxide / ethanol / 6 h / 80 °C

With sodium hydroxide; trichlorophosphate; In ethanol; water;
DOI:10.1016/j.bmcl.2012.12.035