N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

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Chemical Name:N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide
CAS No.:1333320-39-0
Molecular Formula:C₂₃H₂₃FN₆O₃
Molecular Weight:450.472
Hs Code.:

Synonyms:N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

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Chemical Property of N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

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Technology Process of N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

There total 5 articles about N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide 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: 30.3%

: 402-65-3
2-fluoropyridine-4-carboxylic acid

: tert-butyl (2-{4-[5-(benzyloxy)pyrimidin-2-yl]piperazin-1-yl}-2-oxoethyl)carbamate hydrochloride

: 1333320-39-0
N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

Guidance literature:: With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 1333320-39-0
N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / toluene / 24 h / 110 °C / Inert atmosphere

2.1: triethylamine; isobutyl chloroformate / tetrahydrofuran / -15 °C

2.2: -10 - 20 °C

3.1: hydrogenchloride / diethyl ether / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; 1,10-Phenanthroline; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; isobutyl chloroformate; copper(l) iodide; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide; toluene;

Reference yield:

: 99931-82-5
1-(5-bromopyrimidin-2-yl)piperazine

: 1333320-39-0
N-{2-[4-(5-benzyloxy-pyrimidin-2-yl)-piperazin-1-yl]-2-oxo-ethyl}-2-fluoropyridine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / toluene / 24 h / 110 °C / Inert atmosphere

2.1: triethylamine; isobutyl chloroformate / tetrahydrofuran / -15 °C

2.2: -10 - 20 °C

3.1: hydrogenchloride / diethyl ether / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; 1,10-Phenanthroline; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; isobutyl chloroformate; copper(l) iodide; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide; toluene;