2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

Base Information

Chemical Name:2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide
CAS No.:1625677-41-9
Molecular Formula:C₂₇H₂₈ClN₇O₃
Molecular Weight:534.017
Hs Code.:

Synonyms:2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

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Chemical Property of 2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

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Technology Process of 2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

There total 8 articles about 2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide 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: 35.0%

: 1429497-81-3
8-(3-aminophenyl)-2-((2-methoxy-4-(4-methylpiperazin-1-yl)phenyl)amino)pyrido[2,3-d]pyrimidin-7(8H)-one

: 79-04-9
chloroacetyl chloride

: 1625677-41-9
2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 2.41667h;

Reference yield:

: 1363161-14-1
ethyl 4-((3-((tert-butoxycarbonyl)amino)phenyl)amino)-2-(methylthio)pyrimidine-5-carboxylate

: 1625677-41-9
2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 13 h / -40 - 0 °C

2.1: manganese(IV) oxide / chloroform / 18 h / 20 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran; 2-methyltetrahydrofuran / 0.17 h / -78 °C

3.2: 3.17 h / -78 - 20 °C

4.1: peracetic acid / dichloromethane; acetic acid / 0 °C

5.1: N-ethyl-N,N-diisopropylamine / tert-butyl alcohol / 21 h / 80 °C

6.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

7.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2.42 h / 0 °C

With peracetic acid; manganese(IV) oxide; lithium aluminium tetrahydride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; 2-methyltetrahydrofuran; dichloromethane; chloroform; acetic acid; tert-butyl alcohol;

Reference yield:

: 1363161-15-2
tert-butyl 3-(5-(hydroxymethyl)-2-(methylmercapto)pyrimidine-4-ylamino)phenylcarbamate

: 1625677-41-9
2-chloro-N-(3-(2-((2-methoxy-4-(4-methyl-1-piperazinyl)phenyl)amino)-7-oxopyrido[2,3-d]pyrimidin-8(7H)-yl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: manganese(IV) oxide / chloroform / 18 h / 20 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran; 2-methyltetrahydrofuran / 0.17 h / -78 °C

2.2: 3.17 h / -78 - 20 °C

3.1: peracetic acid / dichloromethane; acetic acid / 0 °C

4.1: N-ethyl-N,N-diisopropylamine / tert-butyl alcohol / 21 h / 80 °C

5.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

6.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2.42 h / 0 °C

With peracetic acid; manganese(IV) oxide; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; 2-methyltetrahydrofuran; dichloromethane; chloroform; acetic acid; tert-butyl alcohol;