(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

Base Information

Chemical Name:(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal
CAS No.:1187383-64-7
Molecular Formula:C₃₄H₄₃N₅O₃S₂
Molecular Weight:633.879
Hs Code.:

Synonyms:(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

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Chemical Property of (2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

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Technology Process of (2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

There total 10 articles about (2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal 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:

: 1187383-63-6
(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-nitrobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

: 1187383-64-7
(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

Guidance literature:: With methanol; tin(II) chloride dihdyrate; Reflux;
DOI:10.2174/1573406411309050004

Reference yield:

: 1137-68-4
2-(2'-pyridyl)benzimidazole

: 1187383-64-7
(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 48 h / 20 °C

2: tin(II) chloride dihdyrate; methanol / Reflux

With methanol; tin(II) chloride dihdyrate; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.2174/1573406411309050004

Reference yield:

: 343308-57-6
(2S)-N-[4-(5-bromopentyloxy)-5-methoxy-2-nitrobenzoyl]pyrrolidine-2-carboxaldehyde diethyl thioacetal

: 1187383-64-7
(2S)-N-{4-(5-[2-(2-pyridyl)benzimidazol-1-yl]pentyl)oxy-5-methoxy-2-aminobenzoyl}pyrrolidine-2-carboxaldehyde diethyl thioacetal

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 48 h / 20 °C

2: tin(II) chloride dihdyrate; methanol / Reflux

With methanol; tin(II) chloride dihdyrate; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.2174/1573406411309050004