N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide

Base Information

• Chemical Name: N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide
• CAS No.: 1449110-68-2
• Molecular Formula: C₂₆H₂₅NO₄S
• Molecular Weight: 447.555
• Mol file: 1449110-68-2.mol

Synonyms:N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide

Chemical Property of N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide

There total 1 articles about N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-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:

N-cinnamyl-4-methyl-N-(prop-2-yn-1-yl)-benzenesulfonamide (373640-90-5) + salicylaldehyde (90-02-8) → N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide (1449110-68-2)

Guidance literature:

N-cinnamyl-4-methyl-N-(prop-2-yn-1-yl)-benzenesulfonamide; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 2h; Inert atmosphere;

salicylaldehyde; In tetrahydrofuran; at -78 ℃; for 2h; Inert atmosphere;

DOI:10.1021/acs.orglett.6b00260

Reference yield: 90.0%

N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide (1449110-68-2) → 1-(benzofuran-2-yl)-6-phenyl-3-tosyl-3-azabicyclo[3.1.0]hexane

Guidance literature:

With calcium(II) bis(trifluoromethanesulfonyl)imide; tert-butylammonium hexafluorophosphate(V); In 1,2-dichloro-ethane; at 20 ℃; for 3h; diastereoselective reaction;

DOI:10.1002/anie.201209053

Reference yield: 80.0%

N-cinnamyl-N-(4-hydroxy-4-(2-hydroxyphenyl)but-2-yn-1-yl)-4-methylbenzenesulfonamide (1449110-68-2) → 1-(benzofuran-2-yl)-6-phenyl-3-tosyl-3-azabicyclo[3.1.0]hexane

Guidance literature:

With rhodium(II) pivalate; trifluoroacetic acid; In 1,2-dichloro-ethane; at 80 ℃; for 3h; Inert atmosphere;

DOI:10.1021/acs.orglett.6b00260

upstream raw materials:

N-cinnamyl-4-methyl-N-(prop-2-yn-1-yl)-benzenesulfonamide

salicylaldehyde