tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate
CAS No.:1293396-37-8
Molecular Formula:C₂₃H₂₇N₅O₂
Molecular Weight:405.5
Hs Code.:

Synonyms:tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

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Chemical Property of tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

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Technology Process of tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

There total 3 articles about tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-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: 85.0%

: 1293396-29-8
tert-Butyl 4-{[(1E)-pyrimidin-4-ylmethylene]amino}piperidine-1-carboxylate

: 36635-66-2
α-tosylbenzyl isocyanide

: 1293396-37-8
tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 25746-87-6
acetal dimethylique du pyrimidine-4 carboxaldehyde

: 1293396-37-8
tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / water / 24 h / 60 - 70 °C

2: tert-butyl methyl ether / 2.5 h

3: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

With hydrogenchloride; potassium carbonate; In tert-butyl methyl ether; water; N,N-dimethyl-formamide;

Reference yield:

: 2435-50-9
pyrimidine-4-carboxaldehyde

: 1293396-37-8
tert-Butyl 4-(4-phenyl-5-pyrimidin-4-yl-1H-imidazol-1-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: tert-butyl methyl ether / 2.5 h

2: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

With potassium carbonate; In tert-butyl methyl ether; N,N-dimethyl-formamide;