{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Base Information

Chemical Name:{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol
CAS No.:129163-48-0
Molecular Formula:C₄₀H₅₂BrIO₈
Molecular Weight:867.657
Hs Code.:

{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Synonyms:{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Suppliers and Price of {(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of {(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of {(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

There total 5 articles about {(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol 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:

: 129189-24-8
(2S,3S,4S)-3,4-Bis-benzyloxy-2-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-hydroxy-4-methyl-pentanoic acid methoxy-methyl-amide

: 129163-48-0
{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: pyridinium p-toluenesulfonate / CH₂Cl₂ / 7 h / Ambient temperature

2: lithium aluminum hydride / diethyl ether / 0.5 h / Ambient temperature

3: 1.) n-butyllithium / 1.) tetrahydrofuran, room temperature, 20 min, 2.) -78 deg C --> room temperature

4: 1.) iodine, sodium bicarbonate, 2.) conc. hydrochloric acid / 1.) acetonitrile, 0 deg C, 10 min, 2.) tetrahydrofuran, 20 min, room temperature

With hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; iodine; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(01)97592-1

Reference yield:

: (2S,3S,4S)-3,4-Bis-benzyloxy-2-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-(2-ethoxy-ethoxy)-4-methyl-pentanoic acid methoxy-methyl-amide

: 129163-48-0
{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminum hydride / diethyl ether / 0.5 h / Ambient temperature

2: 1.) n-butyllithium / 1.) tetrahydrofuran, room temperature, 20 min, 2.) -78 deg C --> room temperature

3: 1.) iodine, sodium bicarbonate, 2.) conc. hydrochloric acid / 1.) acetonitrile, 0 deg C, 10 min, 2.) tetrahydrofuran, 20 min, room temperature

With hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; iodine; sodium hydrogencarbonate; In diethyl ether;
DOI:10.1016/S0040-4020(01)97592-1

Reference yield:

: 128041-97-4
C₄₆H₅₅BrO₉

: 129163-48-0
{(2S,3R,4S,5S)-3-Benzyloxy-4-[(1S,2R)-1-benzyloxy-2-((2R,3S,4R,5S)-4-benzyloxy-5-bromomethyl-3,5-dimethyl-tetrahydro-furan-2-yl)-3-methoxymethoxy-propyl]-5-iodomethyl-2-methyl-tetrahydro-furan-2-yl}-methanol

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / CH₂Cl₂ / 16 h / Ambient temperature

2: pyridinium p-toluenesulfonate / CH₂Cl₂ / 7 h / Ambient temperature

3: lithium aluminum hydride / diethyl ether / 0.5 h / Ambient temperature

4: 1.) n-butyllithium / 1.) tetrahydrofuran, room temperature, 20 min, 2.) -78 deg C --> room temperature

5: 1.) iodine, sodium bicarbonate, 2.) conc. hydrochloric acid / 1.) acetonitrile, 0 deg C, 10 min, 2.) tetrahydrofuran, 20 min, room temperature

With hydrogenchloride; lithium aluminium tetrahydride; n-butyllithium; iodine; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4020(01)97592-1