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di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate

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  • Chemical Name:di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate
  • CAS No.:1220627-13-3
  • Molecular Formula:C41H48N6O6
  • Molecular Weight:720.869
  • Hs Code.:
di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate

Synonyms:di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate

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Chemical Property of di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate
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Technology Process of di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate

There total 5 articles about di-tert-butyl 4-((4-(3-(3-tert-butyl-1-p-tolyl-1H-pyrazol-5-yl)ureido) naphthalen-1-yloxy)methyl)pyridin-3-yliminodicarbonate 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: sodium hydride / tetrahydrofuran
2: dmap / ethyl acetate; tetrahydrofuran; 2-Methylpentane
3: acetic acid / Pt/C / methanol
4: CDI / ethyl acetate; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; 2-Methylpentane
With dmap; sodium hydride; CDI; acetic acid; Pt/C; In tetrahydrofuran; methanol; 2-Methylpentane; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; ethyl acetate;
Guidance literature:
Multi-step reaction with 4 steps
1: sodium hydride / tetrahydrofuran
2: dmap / ethyl acetate; tetrahydrofuran; 2-Methylpentane
3: acetic acid / Pt/C / methanol
4: CDI / ethyl acetate; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; 2-Methylpentane
With dmap; sodium hydride; CDI; acetic acid; Pt/C; In tetrahydrofuran; methanol; 2-Methylpentane; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; ethyl acetate;
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