methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

Base Information

Chemical Name:methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate
CAS No.:1451067-49-4
Molecular Formula:C₂₁H₃₁NO₅
Molecular Weight:377.481
Hs Code.:

Synonyms:methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

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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 methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

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Technology Process of methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

There total 3 articles about methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate 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:

: 53403-56-8
Azimsaeure-methylester

: 501-53-1,94274-21-2
benzyl chloroformate

: 1451067-49-4
methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

Guidance literature:: In 1,4-dioxane; water; for 72h;
DOI:10.1016/j.tet.2013.07.083

Reference yield:

: 1451067-48-3
methyl 6-{(2R,5S,6S)-1-[(tert-butoxy)carbonyl]-5-(methoxymethoxy)-6-methylpiperidine-2-yl}hexanoate

: 1451067-49-4
methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / methanol; water / 19 h

2: water; 1,4-dioxane / 72 h

With hydrogenchloride; In 1,4-dioxane; methanol; water;
DOI:10.1016/j.tet.2013.07.083

Reference yield:

: methyl 6-{(2S,5S,6S)-1-[(tert-butoxy)carbonyl]-5-(methoxymethoxy)-6-methylpiperidine-2-yl}hex-5-enoate

: 1451067-49-4
methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 5%-palladium/activated carbon; hydrogen / methanol / 5 h

2: hydrogenchloride / methanol; water / 19 h

3: water; 1,4-dioxane / 72 h

With hydrogenchloride; 5%-palladium/activated carbon; hydrogen; In 1,4-dioxane; methanol; water;
DOI:10.1016/j.tet.2013.07.083