methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside
CAS No.:357399-52-1
Molecular Formula:C₂₄H₃₁NO₇S
Molecular Weight:477.579
Hs Code.:

Synonyms:methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

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Chemical Property of methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

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Technology Process of methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

There total 3 articles about methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-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: 76.0%

: methyl 3-O-benzoyl-4,6-O-benzylidene-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

: 357399-52-1
methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

Guidance literature:: With water; acetic acid; at 65 ℃; for 1h;
DOI:10.1021/jo010210+

Reference yield:

: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-6-acetylsulfanyl-5-[1-(4,4-dimethyl-2,6-dioxo-cyclohexylidene)-ethylamino]-tetrahydro-pyran-4-yl ester

: 357399-52-1
methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium methoxide / methanol / 0.67 h / 20 °C

1.2: 89 percent / methanol / 1 h / 20 °C

2.1: 55 percent / camphorsulfonic acid / 18 h / 20 °C

3.1: 80 percent / pyridine; 4-(dimethylamino)pyridine / 16 h / 20 °C

4.1: 76 percent / acetic acid; water / 1 h / 65 °C

With pyridine; dmap; camphor-10-sulfonic acid; water; sodium methylate; acetic acid; In methanol;
DOI:10.1021/jo010210+

Reference yield:

: 282525-99-9
methyl 4,6-O-benzylidene-2-deoxy-2-N-[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl]amino-1-thio-β-D-glucopyranoside

: 357399-52-1
methyl 3-O-benzoyl-2-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethylamino)-2-deoxy-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / pyridine; 4-(dimethylamino)pyridine / 16 h / 20 °C

2: 76 percent / acetic acid; water / 1 h / 65 °C

With pyridine; dmap; water; acetic acid;
DOI:10.1021/jo010210+