2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

Base Information

Chemical Name:2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate
CAS No.:1391418-78-2
Molecular Formula:C₂HF₃O₂*C₂₅H₂₂Cl₂FN₅O
Molecular Weight:612.411
Hs Code.:

Synonyms:2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

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Chemical Property of 2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

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Technology Process of 2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

There total 7 articles about 2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate 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:

: 1391001-33-4
tert-butyl 4-(4-(2-(2,6-dichlorobenzyl)-5,6-dihydro-5-oxo-1,6-naphthyridin-4-ylamino)-2-fluorophenyl)piperazine-1-carboxylate

: 76-05-1
trifluoroacetic acid

: 1391418-78-2
2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

Guidance literature:: In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 1391001-13-0
methyl 3-amino-4-(2,6-dichlorophenyl)butanoate

: 1391418-78-2
2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

Guidance literature:: Multi-step reaction with 7 steps

1.1: magnesium sulfate; acetic acid / toluene / 3 h / 110 °C

2.1: potassium tert-butylate / tetrahydrofuran / 18 h / 20 °C

3.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / tetrahydrofuran / 18.08 h / 20 °C

4.1: trichlorophosphate / 2.5 h / 102 °C

5.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 20 °C / Inert atmosphere

5.2: 18 h / 100 °C

6.1: toluene-4-sulfonic acid / butan-1-ol / 18 h / 100 °C

7.1: dichloromethane / 18 h / 20 °C

With potassium tert-butylate; sodium hydride; magnesium sulfate; acetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; trichlorophosphate; toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; toluene; butan-1-ol;

Reference yield:

: 1391001-14-1
ethyl 3-(1-(methoxycarbonyl)-3-(2,6-dichlorophenyl)propan-2-ylamino)but-2-enoate

: 1391418-78-2
2-(2,6-dichlorobenzyl)-4-(3-fluoro-4-(piperazin-1-yl)phenylamino)-1,6-naphthyridin-5(6H)-one trifluoroacetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium tert-butylate / tetrahydrofuran / 18 h / 20 °C

2.1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / tetrahydrofuran / 18.08 h / 20 °C

3.1: trichlorophosphate / 2.5 h / 102 °C

4.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 20 °C / Inert atmosphere

4.2: 18 h / 100 °C

5.1: toluene-4-sulfonic acid / butan-1-ol / 18 h / 100 °C

6.1: dichloromethane / 18 h / 20 °C

With potassium tert-butylate; sodium hydride; 2,3-dicyano-5,6-dichloro-p-benzoquinone; trichlorophosphate; toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; butan-1-ol;