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

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Chemical Name:N-butyloxycarbonyl-N,N-bis<<(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidinyl>methyl>amine
CAS No.:231619-05-9
Molecular Formula:C₆₉H₈₅N₃O₁₂
Molecular Weight:1148.45
Hs Code.:

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

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

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

There total 4 articles about N-butyloxycarbonyl-N,N-bis<<(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidinyl>methyl>amine 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: 97.0%

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

: 231619-03-7
N,N-bis<<(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidinyl>methyl>amine

: 231619-05-9
N-butyloxycarbonyl-N,N-bis<<(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidinyl>methyl>amine

Guidance literature:: With triethylamine; In dichloromethane; Ambient temperature;
DOI:10.1021/jo9902446

Reference yield:

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

: 231619-05-9
N-butyloxycarbonyl-N,N-bis<<(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidinyl>methyl>amine

Guidance literature:: Multi-step reaction with 4 steps

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

2: 684.8 mg / Pb(OAc)4 / toluene / 1.5 h / Ambient temperature

3: 75 percent / ammonium acetate, NaBH₃CN / methanol / 22 h / Ambient temperature

4: 97 percent / Et₃N / CH₂Cl₂ / Ambient temperature

With ammonium acetate; lead(IV) acetate; sodium cyanoborohydride; triethylamine; In methanol; dichloromethane; toluene;
DOI:10.1021/jo9902446

Reference yield:

: 231618-87-4
(2S,3R,4R,5R)-N-butyloxycarbonyl-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidine-2-carbaldehyde

: 231619-05-9
N-butyloxycarbonyl-N,N-bis<<(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-<(benzyloxy)methyl>pyrrolidinyl>methyl>amine

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / ammonium acetate, NaBH₃CN / methanol / 22 h / Ambient temperature

2: 97 percent / Et₃N / CH₂Cl₂ / Ambient temperature

With ammonium acetate; sodium cyanoborohydride; triethylamine; In methanol; dichloromethane;
DOI:10.1021/jo9902446