N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

Base Information

Chemical Name:N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide
CAS No.:457638-69-6
Molecular Formula:C₂₁H₂₆N₂O₅S₂
Molecular Weight:450.58
Hs Code.:

<i>N</i>-(2-amino-phenyl)-<i>N</i>-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

Synonyms:N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

Suppliers and Price of N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

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Technology Process of N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

There total 6 articles about N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide 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: 89.0%

: 457638-62-9
N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-N-(2-nitro-phenyl)-methanesulfonamide

: 457638-69-6
N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

Guidance literature:: With copper acetylacetonate; sodium tetrahydroborate; In ethanol;
DOI:10.1021/ol0262643

Reference yield:

: 457638-57-2
N-[(Z)-4-{(Z)-4-hydroxybut-2-enyloxy}but-2-enyl]-N-(2-nitrophenyl)methanesulfonamide

: 457638-69-6
N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: N-bromosuccinimide; dimethyl sulfide / CH₂Cl₂ / 0 - 20 °C

2: sodium hydride / tetrahydrofuran

3: 59 percent / sodium periodate / H₂O; methanol / 20 °C

4: 89 percent / Cu(acac)2; sodium borohydride / ethanol

With copper acetylacetonate; sodium tetrahydroborate; sodium periodate; N-Bromosuccinimide; dimethylsulfide; sodium hydride; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;
DOI:10.1021/ol0262643

Reference yield:

: N-[(Z)-4-{(Z)-4-bromobut-2-enyloxy}but-2-enyl]-N-(2-nitrophenyl)methanesulfonamide

: 457638-69-6
N-(2-amino-phenyl)-N-[4-(4-benzenesulfonyl-but-2-enyloxy)-but-2-enyl]-methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / tetrahydrofuran

2: 59 percent / sodium periodate / H₂O; methanol / 20 °C

3: 89 percent / Cu(acac)2; sodium borohydride / ethanol

With copper acetylacetonate; sodium tetrahydroborate; sodium periodate; sodium hydride; In tetrahydrofuran; methanol; ethanol; water;
DOI:10.1021/ol0262643