1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol

Base Information

Chemical Name:1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol
CAS No.:1644077-51-9
Molecular Formula:C₃₉H₄₈N₄O₁₆S
Molecular Weight:860.893
Hs Code.:

Synonyms:1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol

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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 1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol

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Technology Process of 1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol

There total 1 articles about 1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol 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: 78.0%

: 1381863-30-4
propargyl 3-p-toluenesulfonamido-4-(2’,3’,4’,6’,-tetra-O-acetyl-α-D-glucopyranoside)-6-O-acetyl-2,3-dideoxy-α-D-allopyranoside

: 622-79-7
benzyl azide

: 1644077-51-9
1-benzyl-4-(4'-(2'',3'',4'',6''-tetra-O-acetyl-α-D-allopyranoside)-6'-O-acetyl-2',3'-dideoxy-α-D-allopyranosyloxymethyl)-1H-1,2,3-triazol

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In N,N-dimethyl-formamide; at 70 ℃; for 0.25h; regioselective reaction; Sealed tube; Microwave irradiation;
DOI:10.3762/bjoc.10.134