4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

Base Information

Chemical Name:4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile
CAS No.:351532-18-8
Molecular Formula:C₂₀H₂₀N₂O₂S
Molecular Weight:352.457
Hs Code.:

Synonyms:4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

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Chemical Property of 4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

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Technology Process of 4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

There total 1 articles about 4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-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: 85.0%

: 117601-23-7
4-(4-methoxyphenyl)-2-sulfanylidene-1,2,5,6,7,8-hexahydroquinoline-3-carbonitrile

: 78-95-5
chloroacetone

: 351532-18-8
4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

Guidance literature:: With sodium acetate; In ethanol; for 2h; Heating;

Reference yield: 96.0%

: 351532-18-8
4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

: 351532-25-7
1-[3-amino-4-(4-methoxy-phenyl)-5,6,7,8-tetrahydro-thieno[2,3-b]quinolin-2-yl]-ethanone

Guidance literature:: With sodium ethanolate; In ethanol; for 0.0833333h; Heating;

Reference yield:

: 351532-18-8
4-(4-methoxy-phenyl)-2-(2-oxo-propylsulfanyl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile

: 3,5-bis-(4-methoxy-phenyl)-3,4,6,7,8,9-hexahydro-2H-11-thia-4,10-diaza-benzo[b]fluoren-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / EtONa / ethanol / 0.08 h / Heating

2: 81 percent / NaOH / ethanol / 4 h / 50 - 55 °C

3: 71 percent / 85 percent H₃PO₄; AcOH / 4 h / Heating

With sodium hydroxide; phosphoric acid; sodium ethanolate; acetic acid; In ethanol;