N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

Base Information

Chemical Name:N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide
CAS No.:286420-55-1
Molecular Formula:C₆₃H₇₉NO₁₅
Molecular Weight:1090.32
Hs Code.:

<i>N</i>-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-<i>d</i>][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

Synonyms:N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

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Chemical Property of N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

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Technology Process of N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

There total 6 articles about N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide 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: 74.0%

: 1125-88-8
benzaldehyde dimethyl acetal

: 286420-52-8
N-[(2R,3R,4R,5S,6R)-6-Benzyloxymethyl-2-octyloxy-5-((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-4-((2S,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

: 286420-55-1
N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

Guidance literature:: With toluene-4-sulfonic acid; In acetonitrile; at 20 ℃; for 2h;
DOI:10.1016/S0960-894X(00)00207-9

Reference yield:

: 116514-50-2,128962-63-0,131545-02-3,136758-06-0,99409-34-4,116391-11-8
ethyl 2,3,4-tri-O-benzyl-1-thio-β-L-fucopyranoside

: 286420-55-1
N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 88 percent / CuBr₂; Bu₄NBr / 1,2-dichloro-ethane; dimethylformamide / 24 h / 20 °C

2: 79 percent / NaBH₃CN; HCl*Et₂O / dimethylformamide / 3 h / 0 - 5 °C

3: BF₃*Et₂O / CH₂Cl₂ / 3 h / -10 - 20 °C

4: NaHCO₃; MeONa / methanol

5: 74 percent / p-TsOH / acetonitrile / 2 h / 20 °C

With boron trifluoride diethyl etherate; tetrabutylammomium bromide; sodium methylate; hydrochloric acid diethyl ether; sodium cyanoborohydride; sodium hydrogencarbonate; toluene-4-sulfonic acid; copper(ll) bromide; In methanol; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile; 1: glycosylation / 2: reductive ring opening / 3: glycosylation / 4: Deacetylation / 5: benzylidenation;
DOI:10.1016/S0960-894X(00)00207-9

Reference yield:

: 196876-39-8
1-octyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 286420-55-1
N-[6-benzyloxymethyl-5-(7,8-dihydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2-octyloxy-4-(3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl]-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 88 percent / CuBr₂; Bu₄NBr / 1,2-dichloro-ethane; dimethylformamide / 24 h / 20 °C

2: 79 percent / NaBH₃CN; HCl*Et₂O / dimethylformamide / 3 h / 0 - 5 °C

3: BF₃*Et₂O / CH₂Cl₂ / 3 h / -10 - 20 °C

4: NaHCO₃; MeONa / methanol

5: 74 percent / p-TsOH / acetonitrile / 2 h / 20 °C

With boron trifluoride diethyl etherate; tetrabutylammomium bromide; sodium methylate; hydrochloric acid diethyl ether; sodium cyanoborohydride; sodium hydrogencarbonate; toluene-4-sulfonic acid; copper(ll) bromide; In methanol; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile; 1: glycosylation / 2: reductive ring opening / 3: glycosylation / 4: Deacetylation / 5: benzylidenation;
DOI:10.1016/S0960-894X(00)00207-9