(3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

Base Information

Chemical Name:(3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine
CAS No.:103321-70-6
Molecular Formula:C₂₁H₂₃N₃O₃
Molecular Weight:365.432
Hs Code.:

Synonyms:(3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

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Chemical Property of (3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

Chemical Property:

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Technology Process of (3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

There total 16 articles about (3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine 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: 85.0%

: 143-33-9,25596-52-5
sodium cyanide

: 119719-83-4
(3S,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-<<(p-tolylsulfonyl)oxy>methyl>isoxazolidine

: 103321-70-6
(3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

Guidance literature:: In dimethyl sulfoxide; at 80 ℃; for 4h;
DOI:10.1021/jo00270a037

Reference yield:

: 5041-33-8
N-(Benzyloxycarbonyl)allylamine

: 103321-70-6
(3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

Guidance literature:: Multi-step reaction with 6 steps

1: toluene, reflux, 14 h

2: 10 percent HCl, MeOH / 4 h / 90 °C

3: K₂CO₃ / dimethylformamide / 1 h / 50 °C

4: LiAlH₄ / diethyl ether / 0.5 h / Ambient temperature

5: (iPr)2NEt, Et₃N / CH₂Cl₂ / 10 h / 0 - 25 °C

6: dimethylsulfoxide / rt., 2 h, than 50 deg C, 10 h

With hydrogenchloride; methanol; lithium aluminium tetrahydride; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In diethyl ether; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/ja00275a064

Reference yield:

: 103321-68-2
(3S,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(hydroxymethyl)isoxazolidine

: 103321-70-6
(3R,5R)-N-benzyl-5-<<(benzyloxycarbonyl)amino>methyl>-3-(cyanomethyl)isoxazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: (iPr)2NEt, Et₃N / CH₂Cl₂ / 10 h / 0 - 25 °C

2: dimethylsulfoxide / rt., 2 h, than 50 deg C, 10 h

With triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane; dimethyl sulfoxide;
DOI:10.1021/ja00275a064