methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

Base Information

Chemical Name:methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside
CAS No.:193287-55-7
Molecular Formula:C₃₂H₄₂N₂O₁₁
Molecular Weight:630.692
Hs Code.:

Synonyms:methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

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Chemical Property of methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

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Technology Process of methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

There total 6 articles about methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-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: 89.0%

: 6096-81-7
dimethyl iminodiacetate

: 193287-54-6
methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-succinamido-α-D-glucopyranoside

: 193287-55-7
methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

Guidance literature:: With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In dichloromethane; at 20 ℃; for 4h;
DOI:10.1016/S0008-6215(97)00091-8

Reference yield:

: 17791-36-5
methyl 2,3-di-O-benzyl-α-D-glucopyranoside

: 193287-55-7
methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: tetrabutylammonium hydrogensulfate; NaOH / CH₂Cl₂; H₂O / 1.5 h / 0 °C

2: NaOH / CH₂Cl₂; H₂O / 0 - 20 °C

3: tetramethylurea / dimethylformamide / 1 h / 80 °C / Heating

4: 88 percent / NaOH / dioxane; H₂O / 2 h / 20 °C

5: 89 percent / EEDQ / CH₂Cl₂ / 4 h / 20 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; tetramethylurea; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; 1: Tosylation / 2: Methylation / 3: Substitution / 4: Hydrolysis / 5: Substitution;
DOI:10.1016/S0008-6215(97)00091-8

Reference yield:

: 67776-12-9
methyl 2,3-di-O-benzyl-6-chloro-6-deoxy-α-D-glucopyranoside

: 193287-55-7
methyl 2,3-di-O-benzyl-6-deoxy-4-O-methyl-6-{4-[N,N-bis-(methoxycarbonylmethyl)-amino]-succinamido}-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / NaOH / dioxane

2: 75 percent / tetramethylurea / dimethylformamide / 1 h / 150 °C / Heating

3: 88 percent / NaOH / dioxane; H₂O / 2 h / 20 °C

4: 89 percent / EEDQ / CH₂Cl₂ / 4 h / 20 °C

With sodium hydroxide; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; tetramethylurea; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; 1: Methylation / 2: Substitution / 3: Hydrolysis / 4: Substitution;
DOI:10.1016/S0008-6215(97)00091-8