4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

Base Information

Chemical Name:4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester
CAS No.:373360-06-6
Molecular Formula:C₂₉H₃₆N₄O₉S₂
Molecular Weight:648.758
Hs Code.:

4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

Synonyms:4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

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Chemical Property of 4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

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Technology Process of 4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

There total 5 articles about 4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl 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: 7.0%

: 340756-75-4
N-[5-((1R)-2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide

: 373359-61-6
{4-[4-(4-oxopiperidin-1-yl)phenylsulfamoyl]phenoxy}acetic acid methyl ester

: 373360-06-6
4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/S0968-0896(01)00114-6

Reference yield:

: 170687-82-8
N-{2-(benzyloxy)-5-[(1R)-2-bromo-1-hydroxyethyl]phenyl}methane sulfonamide

: 373360-06-6
4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / NaN₃; NaI / dimethylsulfoxide / 120 h

2: 76 percent / ammonium formate / 10 percent Pd/C / methanol

3: 7 percent / NaBH(OAc)3; acetic acid / dimethylformamide / 20 °C

With sodium azide; ammonium formate; sodium tris(acetoxy)borohydride; acetic acid; sodium iodide; palladium on activated charcoal; In methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(01)00114-6

Reference yield:

: 300345-77-1
N-[5-((1S)-2-azido-1-hydroxyethyl)-2-hydroxyphenyl]methanesulfonamide

: 373360-06-6
4-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylaminophenyl)ethylamino]piperidin-1-yl}phenylsulfamoyl)phenoxyacetic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / ammonium formate / 10 percent Pd/C / methanol

2: 7 percent / NaBH(OAc)3; acetic acid / dimethylformamide / 20 °C

With ammonium formate; sodium tris(acetoxy)borohydride; acetic acid; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0968-0896(01)00114-6