(E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

Base Information

Chemical Name:(E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid
CAS No.:1602487-73-9
Molecular Formula:C₂₁H₂₉NO₅S
Molecular Weight:407.531
Hs Code.:

Synonyms:(E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

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Chemical Property of (E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

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Technology Process of (E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

There total 3 articles about (E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic 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: 58.0%

: 155378-73-7
(2E)-3-[4-(chlorosulfonyl)phenyl]prop-2-enoic acid

: 366014-01-9
(1R,2R)-2-(2-aminoethyl)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptane

: 1602487-73-9
(E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 48h;
DOI:10.1016/j.ejmech.2014.03.025

Reference yield:

: 366013-96-9,324538-17-2,439689-16-4
2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)acetonitrile

: 1602487-73-9
(E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / diethyl ether

2: triethylamine / dichloromethane / 48 h / 0 - 20 °C

With lithium aluminium tetrahydride; triethylamine; In diethyl ether; dichloromethane;
DOI:10.1016/j.ejmech.2014.03.025

Reference yield:

: 7787-20-4,126-21-6
(1R)-fenchone

: 1602487-73-9
(E)-3-(4-(N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)sulfamoyl)phenyl)acrylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.75 h / -85 °C / Inert atmosphere

1.2: 1 h / -85 °C / Inert atmosphere

2.1: lithium aluminium tetrahydride / diethyl ether

3.1: triethylamine / dichloromethane / 48 h / 0 - 20 °C

With lithium aluminium tetrahydride; n-butyllithium; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1016/j.ejmech.2014.03.025