Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester
CAS No.:187147-01-9
Molecular Formula:C₂₅H₃₁NO₁₂S
Molecular Weight:569.587
Hs Code.:

Synonyms:Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

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Chemical Property of Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

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Technology Process of Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

There total 3 articles about Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester 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: 81.0%

: 187147-00-8
p-acrylamidophenyl-2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

: 507-09-5
tiolacetic acid

: 187147-01-9
Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

Guidance literature:: With potassium carbonate; In acetonitrile; for 5h; Ambient temperature;
DOI:10.1016/S0968-0896(96)00177-0

Reference yield:

: 13242-51-8
1-O-p-nitrophenyl-2,3,4,6-tetra-O-acetyl α-D-mannopyranoside

: 187147-01-9
Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / ammonium formate / 10percent Pd/C / methanol / 0.5 h / Ambient temperature

2: 75 percent / Et₃N / CH₂Cl₂ / 0.75 h / Ambient temperature

3: 81 percent / K₂CO₃ / acetonitrile / 5 h / Ambient temperature

With ammonium formate; potassium carbonate; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/S0968-0896(96)00177-0

Reference yield:

: 187146-99-2
p-Aminophenyl-2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

: 187147-01-9
Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-[4-(3-acetylsulfanyl-propionylamino)-phenoxy]-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / Et₃N / CH₂Cl₂ / 0.75 h / Ambient temperature

2: 81 percent / K₂CO₃ / acetonitrile / 5 h / Ambient temperature

With potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1016/S0968-0896(96)00177-0