tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate
CAS No.:1272972-49-2
Molecular Formula:C₂₁H₂₈N₄O₅S
Molecular Weight:448.543
Hs Code.:

Synonyms:tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

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Chemical Property of tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

Chemical Property:

Boiling Point:648.5±65.0 °C(Predicted)
Density:1.271±0.06 g/cm3(Predicted)

Purity/Quality:

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Technology Process of tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

There total 3 articles about tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-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: 52.0%

: 1272973-58-6
4-(5-hydroxypyrimidin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester

: 53606-06-7
4-(methylsulfonyl)benzyl bromide

: 1272972-49-2
tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 40 ℃; for 2h;

Reference yield:

: 374930-88-8
tert-butyl 4-(5-bromopyrimidin-2-yl)piperazine-1-carboxylate

: 1272972-49-2
tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium acetate; palladium diacetate / N,N-dimethyl-formamide / 16 h / 85 °C / Inert atmosphere

2: sodium peroxoborate tetrahydrate / tetrahydrofuran; water / 16 h / 25 °C

3: caesium carbonate / N,N-dimethyl-formamide / 2 h / 40 °C

With sodium peroxoborate tetrahydrate; potassium acetate; palladium diacetate; caesium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1021/jm300310c

Reference yield:

: 940284-98-0
tert-butyl 4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-2-yl]piperazine-1-carboxylate

: 1272972-49-2
tert-butyl 4-(5-{[4-(methylsulfonyl)benzyl]oxy}pyrimidin-2-yl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium peroxoborate tetrahydrate / tetrahydrofuran; water / 16 h / 25 °C

2: caesium carbonate / N,N-dimethyl-formamide / 2 h / 40 °C

With sodium peroxoborate tetrahydrate; caesium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1021/jm300310c