allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

Base Information

Chemical Name:allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside
CAS No.:628281-02-7
Molecular Formula:C₃₇H₄₃N₃O₁₁
Molecular Weight:705.762
Hs Code.:

Synonyms:allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

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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 allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

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Technology Process of allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

There total 16 articles about allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 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: 100.0%

: 628281-00-5
allyl (methyl 2,4-di-O-acetyl-3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

: 628281-02-7
allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

Guidance literature:: With methanol; potassium carbonate;
DOI:10.1016/j.tetlet.2004.03.046

Reference yield:

: 152432-87-6
allyl 2-azido-2-deoxy-α-D-glucopyranoside

: 628281-02-7
allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: (+/-)-camphorsulfonic acid / acetonitrile / 8 h

2: 99 percent / NaH / dimethylformamide / 0.58 h / 0 °C

3: 90 percent / NaBH₃CN; HCl; 4A MS / methyl orange / diethyl ether; tetrahydrofuran / 0.17 h / 0 °C

4: 81 percent / 4A MS; AgOTf / CH₂Cl₂ / 0 °C

5: 90 percent / K₂CO₃ / methanol / 20 °C

With hydrogenchloride; camphor-10-sulfonic acid; silver trifluoromethanesulfonate; sodium hydride; sodium cyanoborohydride; potassium carbonate; methyl orange; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1002/ejoc.200300254

Reference yield:

: 628280-97-7
allyl 2-azido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

: 628281-02-7
allyl (methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-O-2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / NaH / dimethylformamide / 0.58 h / 0 °C

2: 90 percent / NaBH₃CN; HCl; 4A MS / methyl orange / diethyl ether; tetrahydrofuran / 0.17 h / 0 °C

3: 81 percent / 4A MS; AgOTf / CH₂Cl₂ / 0 °C

4: 90 percent / K₂CO₃ / methanol / 20 °C

With hydrogenchloride; silver trifluoromethanesulfonate; sodium hydride; sodium cyanoborohydride; potassium carbonate; methyl orange; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ejoc.200300254