(S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:(S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide
CAS No.:1208307-87-2
Molecular Formula:C₂₄H₂₇NO₆S
Molecular Weight:457.547
Hs Code.:

Synonyms:(S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

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Chemical Property of (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

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Technology Process of (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

There total 8 articles about (S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide 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: 64.0%

: 1208307-84-9
(S)-N-(2-(benzyloxy)-3-methoxybenzyl)-N-(1-(4-(benzyloxy)phenyl)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide

: 1208307-87-2
(S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 2h; under 2585.81 Torr;
DOI:10.1016/j.bmcl.2009.10.115

Reference yield:

: 1208307-81-6
methyl (S)-2-(N-(2-(benzyloxy)-3-methoxybenzyl)-4-methylphenylsulfonamido)-3-(4-(benzyloxy)phenyl)propanoate

: 1208307-87-2
(S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 °C / Inert atmosphere

2: palladium 10% on activated carbon; hydrogen / methanol / 2 h / 2585.81 Torr / Inert atmosphere

With lithium aluminium tetrahydride; palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2013.10.013

Reference yield:

: 175214-62-7
C₂₄H₂₅NO₅S

: 1208307-87-2
(S)-N-(1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl)-N-(2-hydroxy-3-methoxybenzyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 12 h / 0 - 20 °C / Inert atmosphere

2: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 °C / Inert atmosphere

3: palladium 10% on activated carbon; hydrogen / methanol / 2 h / 2585.81 Torr / Inert atmosphere

With lithium aluminium tetrahydride; palladium 10% on activated carbon; hydrogen; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; 1: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2013.10.013