tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

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Chemical Name:tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate
CAS No.:1234349-80-4
Molecular Formula:C₃₄H₃₆N₈O₃
Molecular Weight:604.712
Hs Code.:

Synonyms:tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

There total 4 articles about tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-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:

: 1126403-30-2
tert-butyl 4-{4-[2-(3-hydroxymethylphenyl)pyrimidin-5-yl]-pyrazol-1-yl}piperidine-1-carboxylate

: 1496-84-0
6-anilino-2H-pyridazin-3-one

: 1234349-80-4
tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 18h; Cooling with ice;

Reference yield:

: 1092568-90-5
(3-(5-bromopyrimidin-2-yl)phenyl)methanol

: 1234349-80-4
tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium phosphate tribasic trihydrate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane / 18 h / 80 °C / Inert atmosphere

2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 18 h / 20 °C / Cooling with ice

With potassium phosphate tribasic trihydrate; di-isopropyl azodicarboxylate; triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,2-dimethoxyethane;

Reference yield:

: 87199-15-3
[3-(hydroxymethyl)phenyl]boronic acid

: 1234349-80-4
tert-butyl 4-(4-{2-[3-(6-oxo-3-phenylamino-6H-pyridazin-1-ylmethyl)phenyl]pyrimidin-5-yl}pyrazol-1-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / toluene; ethanol; water / 18 h / 80 °C / Inert atmosphere

2: potassium phosphate tribasic trihydrate / bis-triphenylphosphine-palladium(II) chloride / 1,2-dimethoxyethane / 18 h / 80 °C / Inert atmosphere

3: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 18 h / 20 °C / Cooling with ice

With potassium phosphate tribasic trihydrate; di-isopropyl azodicarboxylate; sodium carbonate; triphenylphosphine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; water; toluene;