(2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

Base Information

Chemical Name:(2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine
CAS No.:1255150-83-4
Molecular Formula:C₃₁H₅₁NO₆Si
Molecular Weight:561.835
Hs Code.:

Synonyms:(2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

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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 (2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

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Technology Process of (2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

There total 1 articles about (2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine 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: 76.0%

: 1255150-71-0
(2S,3S)-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-2-[(1R)-1-methoxycarbonyl-but-3-enyl]piperidine

: 68972-96-3
(Z)-1,4-dibenzyloxy-2-butene

: 1255150-83-4
(2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

Guidance literature:: With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; p-benzoquinone; In toluene; for 0.5h; Reflux; Inert atmosphere;
DOI:10.1021/ol1022257

Reference yield: 100.0%

: 1255150-83-4
(2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pent-3-enyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

: 1255150-84-5
(2S,3S)-2-[(1R)-5-benzyloxy-1-methoxycarbonyl-pentyl]-N-tert-butoxycarbonyl-3-((tert-butyldimethylsiloxy)methyl)-piperidine

Guidance literature:: With palladium 10% on activated carbon; hydrogen; triethylamine; In ethanol; at 20 ℃; for 1h; under 760.051 Torr;
DOI:10.1021/ol1022257