6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

Base Information

Chemical Name:6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid
CAS No.:1569314-60-8
Molecular Formula:C₂₆H₂₄N₂O₆S
Molecular Weight:492.552
Hs Code.:

Synonyms:6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

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Chemical Property of 6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

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Technology Process of 6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

There total 4 articles about 6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic 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:

: 22952-24-5
6-nitrosaccharin

: 1569314-60-8
6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 4 h / 60 - 80 °C

2: hydrogen; palladium 10% on activated carbon / tetrahydrofuran / 4 h / 20 °C / 760.05 Torr

3: sodium hydrogencarbonate / tetrahydrofuran / 8 h / 20 °C

With palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2014.01.045

Reference yield:

: 92-92-2
biphenyl-4-carboxylic acid

: 1569314-60-8
6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride; N,N-dimethyl-formamide / 2 h / 60 °C

2: sodium hydrogencarbonate / tetrahydrofuran / 8 h / 20 °C

With thionyl chloride; sodium hydrogencarbonate; N,N-dimethyl-formamide; In tetrahydrofuran;
DOI:10.1016/j.bmc.2014.01.045

Reference yield:

: 1569314-55-1
6-(6-nitro-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

: 1569314-60-8
6-(6-([1,1'-biphenyl]-4-ylcarboxamido)-1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)hexanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen; palladium 10% on activated carbon / tetrahydrofuran / 4 h / 20 °C / 760.05 Torr

2: sodium hydrogencarbonate / tetrahydrofuran / 8 h / 20 °C

With palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; In tetrahydrofuran;
DOI:10.1016/j.bmc.2014.01.045