1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

Base Information

Chemical Name:1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile
CAS No.:1356152-69-6
Molecular Formula:C₂₇H₂₂FN₃O₂S
Molecular Weight:471.555
Hs Code.:

Synonyms:1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

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Chemical Property of 1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

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Technology Process of 1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

There total 4 articles about 1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile 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: 42.0%

: 749865-60-9
4-chloro-1-(4-fluorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carbonitrile

: 86542-98-5
piperidin-4-yl(thiophen-2-yl)methanone

: 1356152-69-6
1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

Guidance literature:: With triethylamine; In toluene; for 8h; Reflux;

Reference yield:

: 118-48-9
isatoic anhydride

: 1356152-69-6
1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h

1.2: 1 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1.5 h / 20 °C

2.2: 0.5 h

3.1: methanesulfonyl chloride; lithium chloride / N,N-dimethyl acetamide / 2 h / 20 °C

4.1: triethylamine / toluene / 8 h / Reflux

With sodium hydride; methanesulfonyl chloride; triethylamine; lithium chloride; In N,N-dimethyl acetamide; N,N-dimethyl-formamide; toluene; mineral oil;

Reference yield:

: 40534-52-9
N-(4-fluorobenzyl)isatoic anhydride

: 1356152-69-6
1-(4-fluorobenzyl)-2-oxo-4-[4-(thiophen-2ylcarbonyl)piperidin-1-yl]-1,2-dihydroquinoline-3-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1.5 h / 20 °C

1.2: 0.5 h

2.1: methanesulfonyl chloride; lithium chloride / N,N-dimethyl acetamide / 2 h / 20 °C

3.1: triethylamine / toluene / 8 h / Reflux

With sodium hydride; methanesulfonyl chloride; triethylamine; lithium chloride; In N,N-dimethyl acetamide; N,N-dimethyl-formamide; toluene; mineral oil;