N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

Base Information

Chemical Name:N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide
CAS No.:271588-09-1
Molecular Formula:C₁₉H₂₇Cl₃N₂O₈
Molecular Weight:517.791
Hs Code.:

Synonyms:N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

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Chemical Property of N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

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Technology Process of N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

There total 3 articles about N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide 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:

: 271588-03-5
endo-4-O-Cyclohexylcarbamoyl-6-O-formyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl azide

: 271588-09-1
N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / Et₃N / methanol / 0.17 h / Heating

2: PPh₃; pyridine / 2 h / 20 °C

3: pyridine / 12 h / 20 °C

With pyridine; triethylamine; triphenylphosphine; In methanol; 1: Substitution / 2: Reduction / 3: Acetylation;
DOI:10.1055/s-2000-6250

Reference yield:

: 108-24-7
acetic anhydride

: Cyclohexyl-carbamic acid (2S,3aR,4R,6R,7S,7aR)-4-amino-6-hydroxymethyl-2-trichloromethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester

: 271588-09-1
N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

Guidance literature:: With pyridine; at 20 ℃; for 12h;
DOI:10.1055/s-2000-6250

Reference yield:

: 271588-02-4
endo-4-O-Cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl azide

: 271588-09-1
N-[6-O-Acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D-gulopyranosyl]acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: PPh₃; pyridine / 2 h / 20 °C

2: pyridine / 12 h / 20 °C

With pyridine; triphenylphosphine; 1: Reduction / 2: Acetylation;
DOI:10.1055/s-2000-6250