(2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

Base Information

Chemical Name:(2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid
CAS No.:1393733-77-1
Molecular Formula:C₂₄H₃₀N₂O₇S
Molecular Weight:490.577
Hs Code.:

Synonyms:(2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

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Chemical Property of (2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

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Technology Process of (2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

There total 8 articles about (2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid 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: 54.0%

: C₂₅H₃₂N₂O₇S

: 1393733-77-1
(2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

Guidance literature:: With water; sodium hydroxide; In acetone; for 0.0833333h;
DOI:10.1124/dmd.111.040428

Reference yield:

: 319926-20-0
(2S,3S,4S,5R,6S)-3,4,5-Triacetoxy-6-aminooxy-tetrahydro-pyran-2-carboxylic acid methyl ester

: 1393733-77-1
(2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: sodium cyanoborohydride; acetic acid / tetrahydrofuran / 21 h / 45 °C

2: sodium methylate / methanol / 1 h / Inert atmosphere

3: water; sodium hydroxide / acetone / 0.08 h

With water; sodium methylate; sodium cyanoborohydride; acetic acid; sodium hydroxide; In tetrahydrofuran; methanol; acetone;
DOI:10.1124/dmd.111.040428

Reference yield:

: (2S,3S,4S,5R,6S)-3,4,5-triacetoxy-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-tetrahydro-pyran-2-carboxylic acid methyl ester

: 1393733-77-1
(2S,3S,4S,5R,6S)-6-{4-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazin-1-yloxy}-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / methanol / 1 h / Inert atmosphere

2: water; sodium hydroxide / acetone / 0.08 h

With water; sodium methylate; sodium hydroxide; In methanol; acetone;
DOI:10.1124/dmd.111.040428