benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside

Base Information

Chemical Name:benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside
CAS No.:174151-35-0
Molecular Formula:C₂₉H₃₁NO₉S
Molecular Weight:569.632
Hs Code.:

Synonyms:benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-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 benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside

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Technology Process of benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside

There total 2 articles about benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-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: 84.0%

: 174151-34-9
benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-6-bromo-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside

: 174151-35-0
benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside

Guidance literature:: With azobisisobutyronitrile; tri-n-butyl-tin hydride; In benzene; for 3h; Heating;
DOI:10.1016/0008-6215(95)00291-X

Reference yield:

: 2864-17-7
benzyl O⁴,O⁶-(R)-benzylidene-2-benzyloxycarbonylamino-O³-methanesulfonyl-α-D-2-deoxy-glucopyranoside

: 174151-35-0
benzyl 4-O-benzoyl-2-benzyloxycarbonylamino-2,6-dideoxy-3-O-methanesulfonyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 41 percent / BaCO₃, NBS / CCl₄; various solvent(s) / 2 h / Heating

2: 84 percent / tributyltin hydride, α,α'-azobisisobutyronitrile / benzene / 3 h / Heating

With N-Bromosuccinimide; azobisisobutyronitrile; tri-n-butyl-tin hydride; barium carbonate; In tetrachloromethane; benzene;
DOI:10.1016/0008-6215(95)00291-X