methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside

Base Information

Chemical Name:methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside
CAS No.:894428-26-3
Molecular Formula:C₂₄H₃₁NO₅S₂
Molecular Weight:477.646
Hs Code.:

Synonyms:methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-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 methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside

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Technology Process of methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside

There total 1 articles about methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-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: 68.0%

: Ziram

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

: 894428-26-3
methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In toluene; at 20 ℃;
DOI:10.1016/j.tet.2006.03.023

Reference yield: 90.0%

: 894428-26-3
methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside

: 604757-18-8
methyl 2,3-di-O-benzyl-6-thio-α-D-glucopyranoside

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 4h; Heating;
DOI:10.1016/j.tet.2006.03.023

Reference yield:

: 894428-26-3
methyl 2,3-di-O-benzyl-6-S-(N,N-dimethyldithiocarbamoyl)-6-thio-α-D-glucopyranoside

: (2S,4aS,6S,7R,8R,8aS)-2-Benzenesulfonylmethyl-6-methoxy-hexahydro-pyrano[2,3-e][1,3]oxathiine-7,8-diol

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / LiAlH₄ / diethyl ether / 4 h / Heating

2: 91 percent / Et₃N; Bu₄NBr / tetrahydrofuran / 12 h / 20 °C

3: 52 percent / NaH; Bu₄NBr / tetrahydrofuran / 12 h / 20 °C

4: trifluoroacetic acid; water / 24 h / 60 °C

With lithium aluminium tetrahydride; tetrabutylammomium bromide; water; sodium hydride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; diethyl ether; 2: Michael addition;
DOI:10.1016/j.tet.2006.03.023