methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

Base Information

Chemical Name:methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate
CAS No.:130087-26-2
Molecular Formula:C₂₆H₃₄N₂O₁₃
Molecular Weight:582.562
Hs Code.:

Synonyms:methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

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Chemical Property of methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

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Technology Process of methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

There total 6 articles about methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate 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: 84.0%

: 59694-37-0
methyl (4-nitrophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

: 130087-26-2
methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

Guidance literature:: With hydrogen; platinum(IV) oxide; In ethyl acetate; for 2h; Ambient temperature;
DOI:10.1248/cpb.39.255

Reference yield:

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

: 130087-26-2
methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / tetrabutylammonium hydrogensulfate (TBAHS), aq. 1M NaOH / CH₂Cl₂ / 25 °C

2: HCOONH₄ / 10percent Pd-C / methanol / 0.08 h / Heating

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

Reference yield:

: 67670-69-3
N-acetyl-4,7,8,9-tetra-O-acetyl-2-chloro-2-deoxyneuraminic acid methyl ester

: 130087-26-2
methyl (4-aminophenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-oxy-α-D-glycero-D-galacto-2-nonulopyranosid)onate

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / tetrabutylammonium hydrogensulfate (TBAHS), aq. 1M NaOH / CH₂Cl₂ / 25 °C

2: HCOONH₄ / 10percent Pd-C / methanol / 0.08 h / Heating

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