1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

Base Information

Chemical Name:1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide
CAS No.:1453114-73-2
Molecular Formula:C₂₂H₂₅N₃O
Molecular Weight:347.46
Hs Code.:

Synonyms:1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

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Chemical Property of 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

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Technology Process of 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

There total 6 articles about 1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide 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: 80.0%

: 1453114-71-0
1-[(2S)-N-benzylpyrrolidin-2-yl]-N-methylidenemethanamine

: 119-51-7
1-phenyl-1,2-propanedione 2-oxime

: 1453114-73-2
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

Guidance literature:: With acetic acid; In ethanol; at 20 ℃; for 24h;
DOI:10.1016/j.tetasy.2013.07.013

Reference yield:

: 31795-93-4
N-benzyl-L-proline

: 1453114-73-2
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

2.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran / 8.17 h / Reflux

3.1: hydrazine / ethanol / 2 h / Reflux

3.2: 0.5 h / Heating

4.1: methanol / 20 °C

5.1: acetic acid / ethanol / 24 h / 20 °C

With lithium aluminium tetrahydride; acetic acid; triphenylphosphine; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol;
DOI:10.1016/j.tetasy.2013.07.013

Reference yield:

: 100-44-7
benzyl chloride

: 1453114-73-2
1-{[(2S)-N-benzylpyrrolidin-2-yl]methyl}-4-methyl-5-phenyl-1H-imidazole 3-oxide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium hydroxide / isopropyl alcohol

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

3.1: diethylazodicarboxylate; triphenylphosphine / tetrahydrofuran / 8.17 h / Reflux

4.1: hydrazine / ethanol / 2 h / Reflux

4.2: 0.5 h / Heating

5.1: methanol / 20 °C

6.1: acetic acid / ethanol / 24 h / 20 °C

With lithium aluminium tetrahydride; acetic acid; triphenylphosphine; potassium hydroxide; hydrazine; diethylazodicarboxylate; In tetrahydrofuran; methanol; ethanol; isopropyl alcohol;
DOI:10.1016/j.tetasy.2013.07.013