p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

Base Information

Chemical Name:p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside
CAS No.:65907-85-9
Molecular Formula:C₂₀H₂₆N₂O₉
Molecular Weight:438.434
Hs Code.:

Synonyms:p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-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 p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

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Technology Process of p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

There total 5 articles about p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-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: 98.0%

: 13089-27-5,13089-23-1
p-nitrophenyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-β-D-glucopyranoside

: 65907-85-9
p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

Guidance literature:: With ammonium formate; palladium on activated charcoal; In methanol; for 0.0333333h; Heating;

Reference yield:

: 3068-34-6
Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester

: 65907-85-9
p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 46.2 percent / Et₃N / acetonitrile / 4 h / 40 °C

2: 91.3 percent / H₂ / 10percent Pd/C / ethanol; dioxane / 3 h / 760 Torr / Ambient temperature

With hydrogen; triethylamine; palladium on activated charcoal; In 1,4-dioxane; ethanol; acetonitrile;
DOI:10.1248/cpb.43.266

Reference yield:

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 65907-85-9
p-aminophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / tetrabutylammonium hydrogen sulfate, 1M NaOH / CH₂Cl₂ / 0.75 h / Ambient temperature

2: 98 percent / ammonium formate / 10percent Pd/C / methanol / 0.03 h / Heating

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; ammonium formate; palladium on activated charcoal; In methanol; dichloromethane;