methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

Base Information

Chemical Name:methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside
CAS No.:592527-09-8
Molecular Formula:C₁₆H₁₉NO₆
Molecular Weight:321.33
Hs Code.:

Synonyms:methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

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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 methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

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Technology Process of methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

There total 1 articles about methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside 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: 86.0%

: 71184-91-3
methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-epimino-α-D-allopyranoside

: 79-22-1
methyl chloroformate

: 592527-09-8
methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/ol035036l

Reference yield: 88.0%

: 592527-09-8
methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

: 592527-13-4
methyl 2-azido-4,6-O-benzylidene-2,3-dideoxy-3-methoxycarbonylamino-α-D-altropyranoside

Guidance literature:: With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; for 4h; Heating;
DOI:10.1021/ol035036l

Reference yield:

: 592527-09-8
methyl 4,6-O-benzylidene-2,3-dideoxy-2,3-(N-methoxycarbonyl)epimino-α-D-allopyranoside

: 592527-04-3
methyl 4,6-O-benzylidene-2,3-dideoxy-3-methoxycarbonylamino-2-trimethylsilylethylsulfonamido-α-D-altropyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / NaN₃; NH₄Cl / dimethylformamide / 4 h / Heating

2: 95 percent / H₂ / Pd(OH)2/C / methanol / 3 h / 20 °C / 760 Torr

3: 61 percent / AgCN / benzene / 22 h / 75 °C

With sodium azide; silver cyanide; hydrogen; ammonium chloride; palladium dihydroxide; In methanol; N,N-dimethyl-formamide; benzene; 1: Furst-Plattner ring-opening;
DOI:10.1021/ol035036l