N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine

Base Information

Chemical Name:N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine
CAS No.:708208-62-2
Molecular Formula:C₂₁H₂₇N₅O₃
Molecular Weight:397.477
Hs Code.:

Synonyms:N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine

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Technology Process of N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine

There total 10 articles about N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine 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: 65.0%

: 708208-66-6
4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzonitrile

: 708208-62-2
N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine

Guidance literature:: With hydroxylamine hydrochloride; potassium carbonate; In ethanol; for 18h; Heating / reflux;

Reference yield:

: 5164-76-1
dimethyl glutaconate

: 708208-62-2
N-hydroxy-4-[3-methyl-5-(2-oxo-3-pyridin-4-yl-imidazolidin-1-yl)-pentyloxy]-benzamidine

Guidance literature:: Multi-step reaction with 6 steps

1.1: CuI / tetrahydrofuran / 20 °C

1.2: TMSCl / tetrahydrofuran / -78 - 20 °C

2.1: lithium aluminum hydride / tetrahydrofuran / 24 h / Heating

3.1: pyridine / 2 h / 20 °C

4.1: 0.83 g / K₂CO₃ / acetonitrile / 24 h / 60 °C

5.1: 91 percent / NaH / dimethylformamide / 20 °C

6.1: NH₂OH*HCl; K₂CO₃ / ethanol / 2 h / Heating

With pyridine; copper(l) iodide; lithium aluminium tetrahydride; hydroxylamine hydrochloride; sodium hydride; potassium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; acetonitrile; 1.2: Michael addition;
DOI:10.1021/jm050033v