(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Base Information

Chemical Name:(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine
CAS No.:231618-92-1
Molecular Formula:C₃₂H₄₀N₂O₅
Molecular Weight:532.68
Hs Code.:

Synonyms:(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

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

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

There total 9 articles about (2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-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:

: 231618-91-0
(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(azidomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

: 231618-92-1
(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 1.5h; Ambient temperature;
DOI:10.1021/jo9902446

Reference yield:

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

: 231618-92-1
(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) LiAlH₄, 2.) Et₃N / 1.) THF, 2.) CH₂Cl₂

2: 424 mg / Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

3: 65 percent / NaN₃ / dimethylformamide / 35 h / 70 °C

4: 59 mg / H₂ / 5 percent Pd on C / methanol / 1.5 h / Ambient temperature

With lithium aluminium tetrahydride; sodium azide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo9902446

Reference yield:

: 159063-89-5
(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidino<1,2-c>oxazole-3-one

: 231618-92-1
(2R,3R,4R,5R)-N-butyloxycarbonyl-2-(aminomethyl)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) LiAlH₄, 2.) Et₃N / 1.) THF, 2.) CH₂Cl₂

2: 424 mg / Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

3: 65 percent / NaN₃ / dimethylformamide / 35 h / 70 °C

4: 59 mg / H₂ / 5 percent Pd on C / methanol / 1.5 h / Ambient temperature

With lithium aluminium tetrahydride; sodium azide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo9902446