methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

Base Information

Chemical Name:methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside
CAS No.:158975-59-8
Molecular Formula:C₃₅H₄₃NO₈
Molecular Weight:605.728
Hs Code.:

Synonyms:methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

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Chemical Property of methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

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Technology Process of methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

There total 3 articles about methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside 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: 60.0%

: 158975-57-6
methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethyl-N-tosylcarbamoyl)-2-deoxy-β-D-galactopyranoside

: 158975-59-8
methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

Guidance literature:: With sodium naphthalenide; In 1,2-dimethoxyethane; at -30 ℃; for 0.333333h;
DOI:10.1016/0008-6215(94)84216-7

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 158975-59-8
methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / KOH, Bu₄NBr / benzene / 4 h / Ambient temperature

2: 60 percent / sodium naphthalenide / 1,2-dimethoxy-ethane / 0.33 h / -30 °C

With potassium hydroxide; tetrabutylammomium bromide; sodium naphthalenide; In 1,2-dimethoxyethane; benzene;
DOI:10.1016/0008-6215(94)84216-7

Reference yield:

: 135735-82-9
methyl 3,4,6-tri-O-benzyl-2-deoxy-2-C-(tosylcarbamoyl)-β-D-galactopyranoside

: 158975-59-8
methyl 3,4,6-tri-O-benzyl-2-C-(N-tert-butoxycarbonylmethylcarbamoyl)-2-deoxy-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / KOH, Bu₄NBr / benzene / 4 h / Ambient temperature

2: 60 percent / sodium naphthalenide / 1,2-dimethoxy-ethane / 0.33 h / -30 °C

With potassium hydroxide; tetrabutylammomium bromide; sodium naphthalenide; In 1,2-dimethoxyethane; benzene;
DOI:10.1016/0008-6215(94)84216-7