(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

Base Information

Chemical Name:(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine
CAS No.:1427173-70-3
Molecular Formula:C₁₅H₂₂N₂O₅
Molecular Weight:310.35
Hs Code.:

Synonyms:(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

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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 (2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

Chemical Property:

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Technology Process of (2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

There total 3 articles about (2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine 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: 40.0%

: 129492-51-9,129492-77-9
(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-((phenylamino)methyl)pyrrolidine

: 141-43-5
ethanolamine

: 1427173-70-3
(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

Guidance literature:: With acetic acid; In methanol; at 20 ℃; for 2h;
DOI:10.1039/c3ob27343a

Reference yield:

: 67561-03-9
N-benzyloxycarbonylglycinal

: 1427173-70-3
(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

Guidance literature:: Multi-step reaction with 3 steps

1.1: D-fructose-6-phosphate aldolase mutant A₁₆₅G / N,N-dimethyl-formamide / 24 h / 25 °C / pH 7 / Enzymatic reaction

1.2: 2585.81 Torr

2.1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / 3.5 h / 40 °C

3.1: acetic acid / methanol / 2 h / 20 °C

With D-fructose-6-phosphate aldolase mutant A₁₆₅G; acetic acid; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In methanol; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1039/c3ob27343a

Reference yield:

: 105878-97-5
(2R,3R,4R)-N-benzyloxycarbonyl-2-(hydroxymethyl)pyrrolidine-3,4-diol

: 1427173-70-3
(2R,3R,4R)-N-benzyloxycarbonyl-3,4-dihydroxy-2-(((2-hydroxyethyl)amino)methyl)pyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / 3.5 h / 40 °C

2: acetic acid / methanol / 2 h / 20 °C

With acetic acid; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In methanol; ethyl acetate;
DOI:10.1039/c3ob27343a