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N-(3-(7-(4-(dimethylamino)-2-methoxyphenylamino)-3-methyl-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl)phenyl)acrylamide

Base Information
  • Chemical Name:N-(3-(7-(4-(dimethylamino)-2-methoxyphenylamino)-3-methyl-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl)phenyl)acrylamide
  • CAS No.:1363160-91-1
  • Molecular Formula:C25H27N7O3
  • Molecular Weight:473.534
  • Hs Code.:
N-(3-(7-(4-(dimethylamino)-2-methoxyphenylamino)-3-methyl-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl)phenyl)acrylamide

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Chemical Property of N-(3-(7-(4-(dimethylamino)-2-methoxyphenylamino)-3-methyl-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl)phenyl)acrylamide
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Technology Process of N-(3-(7-(4-(dimethylamino)-2-methoxyphenylamino)-3-methyl-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl)phenyl)acrylamide

There total 11 articles about N-(3-(7-(4-(dimethylamino)-2-methoxyphenylamino)-3-methyl-2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidin-1(2H)-yl)phenyl)acrylamide 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 3 h / 20 °C
2: trifluoroacetic acid / iso-butanol / 18 h / 110 °C
3: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
4: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C
With N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In dichloromethane; iso-butanol;
DOI:10.1021/jm201591k
Guidance literature:
Multi-step reaction with 10 steps
1: potassium carbonate / N,N-dimethyl-formamide / 80 °C
2: lithium aluminium tetrahydride / tetrahydrofuran / -40 - 20 °C
3: manganese(IV) oxide / dichloromethane / 20 °C
4: sodium acetate / methanol / 1 h / 20 °C
5: sodium tetrahydroborate / methanol / 20 °C
6: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 1 h / 0 - 20 °C
7: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 3 h / 20 °C
8: trifluoroacetic acid / iso-butanol / 18 h / 110 °C
9: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
10: N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C
With manganese(IV) oxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium acetate; potassium carbonate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; iso-butanol;
DOI:10.1021/jm201591k
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