(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Base Information

Chemical Name:(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine
CAS No.:231619-00-4
Molecular Formula:C₄₀H₄₈N₂O₆
Molecular Weight:652.831
Hs Code.:

Synonyms:(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

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Chemical Property of (1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

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Technology Process of (1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

There total 7 articles about (1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)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:

: 231618-99-8
(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-azido-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

: 231619-00-4
(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 1h; Ambient temperature;
DOI:10.1021/jo9902446

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 231619-00-4
(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Guidance literature:: Multi-step reaction with 5 steps

1: 91 percent / Et₃N / CH₂Cl₂ / 20 h / Ambient temperature

2: 85 percent / pyridine / 37 h / Ambient temperature

3: 69 percent / NaN₃ / dimethylformamide / 4 h / 70 °C

4: 93 percent / Ag₂O, KI / dimethylformamide / 7 h / Ambient temperature

5: 25 mg / H₂ / 5 percent Pd on C / methanol / 1 h / Ambient temperature

With sodium azide; hydrogen; triethylamine; potassium iodide; silver(l) oxide; palladium on activated charcoal; In pyridine; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo9902446

Reference yield:

: 231619-09-3
(2R,3S,4S,5R,6R)-6-azido-2,3-epoxy-4,5,7-tris(benzyloxy)-2(E)-hepten-1-ol

: 231619-00-4
(1'R,2R,3R,4R,5R)-N-butyloxycarbonyl-2-<2-amino-1-(benzyloxy)ethyl>-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Guidance literature:: Multi-step reaction with 6 steps

1: 91 percent / PPh₃ / tetrahydrofuran; H₂O / 48 h / Ambient temperature

2: 91 percent / Et₃N / CH₂Cl₂ / 20 h / Ambient temperature

3: 85 percent / pyridine / 37 h / Ambient temperature

4: 69 percent / NaN₃ / dimethylformamide / 4 h / 70 °C

5: 93 percent / Ag₂O, KI / dimethylformamide / 7 h / Ambient temperature

6: 25 mg / H₂ / 5 percent Pd on C / methanol / 1 h / Ambient temperature

With sodium azide; hydrogen; triethylamine; triphenylphosphine; potassium iodide; silver(l) oxide; palladium on activated charcoal; In tetrahydrofuran; pyridine; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo9902446