(2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide

Base Information

Chemical Name:(2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide
CAS No.:1207668-86-7
Molecular Formula:Br*C₃₁H₄₁N₄O₄
Molecular Weight:613.595
Hs Code.:

Synonyms:(2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide

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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 (2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide

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Technology Process of (2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide

There total 1 articles about (2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide 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: 95.0%

: 1207668-84-5
benzyl (2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine-1-carboxylate bromide

: 1207668-86-7
(2S,4R)-4-(5-(1-methyl-1H-imidazol-3-ium-3-yl)pentanoyloxy)-2-[(S)-1-(hydroxy-diphenyl-methyl)-2-methyl-propylcarbamoyl]-pyrrolidine bromide

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 3h; under 760 Torr;
DOI:10.1016/j.tet.2009.11.033