(R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

Base Information

Chemical Name:(R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester
CAS No.:259726-51-7
Molecular Formula:C₃₁H₄₉NO₉
Molecular Weight:579.731
Hs Code.:

(R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

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Chemical Property of (R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

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Technology Process of (R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

There total 1 articles about (R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester 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:

: 100-39-0
benzyl bromide

: (R)-2-[(2R,3S,5R,6S)-6-(tert-Butoxycarbonylamino-methyl)-3-carboxymethoxy-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

: 259726-51-7
(R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

Guidance literature:: With potassium carbonate; Yield given;
DOI:10.1016/S0960-894X(98)00575-7

Reference yield:

: 259726-51-7
(R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

: (S)-3-((R)-2-{(2R,3S,5R,6S)-6-[((S)-2-Acetylamino-3-phenyl-propionylamino)-methyl]-3-carboxymethoxy-5-isobutoxy-tetrahydro-pyran-2-yl}-propionylamino)-N-((S)-1-carboxy-2-phenyl-ethyl)-succinamic acid

Guidance literature:: Multi-step reaction with 6 steps

1: TFA, anisole

2: TEA

3: 88 percent / DEPC, TEA / tetrahydrofuran

4: TFA, anisole

5: 85 percent / DEPC, TEA / tetrahydrofuran

6: 70 percent / H₂ / Pd/C / ethanol

With TEA; hydrogen; methoxybenzene; diethyl dicarbonate; trifluoroacetic acid; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1016/S0960-894X(98)00575-7

Reference yield:

: 259726-51-7
(R)-2-[(2R,3S,5R,6S)-3-Benzyloxycarbonylmethoxy-6-(tert-butoxycarbonylamino-methyl)-5-isobutoxy-tetrahydro-pyran-2-yl]-propionic acid tert-butyl ester

: (S)-3-[(R)-2-((2R,3S,5R,6S)-6-Aminomethyl-3-benzyloxycarbonylmethoxy-5-isobutoxy-tetrahydro-pyran-2-yl)-propionylamino]-N-((S)-1-benzyloxycarbonyl-2-phenyl-ethyl)-succinamic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: TFA, anisole

2: TEA

3: 88 percent / DEPC, TEA / tetrahydrofuran

4: TFA, anisole

With TEA; methoxybenzene; diethyl dicarbonate; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1016/S0960-894X(98)00575-7