ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

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Chemical Name:ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate
CAS No.:1443237-62-4
Molecular Formula:C₂₅H₃₂N₄O₄Si
Molecular Weight:480.639
Hs Code.:

Synonyms:ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

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Chemical Property of ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

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Technology Process of ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

There total 5 articles about ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate 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:

: 900254-92-4
2-(([tert-butyl(dimethyl)silyl]oxy)methyl)prop-2-enoic acid

: 1443234-84-1
ethyl 4-(3-aminophenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

: 1443237-62-4
ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

Guidance literature:: With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In tetrahydrofuran; at 25 ℃; Inert atmosphere;

Reference yield:

: 22276-95-5
5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine

: 1443237-62-4
ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 3.5 h / -78 °C / Inert atmosphere

1.2: 14.5 h / -78 - 30 °C / Inert atmosphere

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; sodium carbonate / N,N-dimethyl-formamide / 1.5 h / 115 °C / Inert atmosphere

3.1: ; hydrogen / dichloromethane; methanol

4.1: triethylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / tetrahydrofuran / 25 °C / Inert atmosphere

With n-butyllithium; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; hydrogen; sodium carbonate; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In tetrahydrofuran; methanol; hexane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1443237-43-1
ethyl 4-(3-nitrophenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

: 1443237-62-4
ethyl 4-(3-((2-((tert-butyl(dimethyl)silyl)oxy)methyl)acryloyl)amino)phenyl-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: ; hydrogen / dichloromethane; methanol

2: triethylamine; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / tetrahydrofuran / 25 °C / Inert atmosphere

With hydrogen; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In tetrahydrofuran; methanol; dichloromethane;