2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

Base Information

Chemical Name:2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one
CAS No.:1356352-54-9
Molecular Formula:C₁₈H₁₆F₃N₃O₃S
Molecular Weight:411.405
Hs Code.:

Synonyms:2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

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Chemical Property of 2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

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Technology Process of 2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

There total 8 articles about 2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one 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:

: 1356353-35-9
7-methoxy-2-thioxo-3-[4-(2,2,2-trifluoroethoxy)phenyl]-2,3-dihydropyrido[2,3-d]pyrimidin-4(1H)-one

: 75-03-6
ethyl iodide

: 1356352-54-9
2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

Guidance literature:: With sodium hydrogencarbonate; In water; acetonitrile; at 100 ℃; for 1h;

Reference yield:

: 65515-28-8
methyl 2,6-dichloronicotinate

: 1356352-54-9
2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: copper(l) iodide; sodium hydrogencarbonate / N,N-dimethyl-formamide / 1.5 h / 80 °C

2.1: trifluoroacetic acid / 2 h / 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / Cooling with ice

3.3: 0.5 h / Reflux

4.1: sodium hydrogencarbonate / water; acetonitrile / 1 h / 100 °C

With copper(l) iodide; sodium hydride; sodium hydrogencarbonate; trifluoroacetic acid; In water; N,N-dimethyl-formamide; acetonitrile; mineral oil;

Reference yield:

: 1356353-33-7
methyl 6-chloro-2-[(4-methoxybenzyl)amino]pyridine-3-carboxylate

: 1356352-54-9
2-(ethylsulfanyl)-7-methoxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]pyrido[2,3-d]pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid / 2 h / 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / Cooling with ice

2.3: 0.5 h / Reflux

3.1: sodium hydrogencarbonate / water; acetonitrile / 1 h / 100 °C

With sodium hydride; sodium hydrogencarbonate; trifluoroacetic acid; In water; N,N-dimethyl-formamide; acetonitrile; mineral oil;