4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

Base Information

Chemical Name:4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide
CAS No.:1416895-64-1
Molecular Formula:C₂₁H₂₃NO₃S
Molecular Weight:369.485
Hs Code.:

Synonyms:4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

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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 4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

Chemical Property:

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Technology Process of 4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

There total 2 articles about 4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide 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:

: 19967-55-6
1-bromo-3-methyl-2-butanone

: 305837-95-0
4-methyl-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

: 1416895-64-1
4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetone; at 20 - 50 ℃; for 24h;
DOI:10.1002/chem.202100143

Reference yield:

: 55022-46-3
4-methyl-N-prop-2-ynylbenzenesulfonamide

: 1416895-64-1
4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / tetrahydrofuran / 20 °C / Inert atmosphere

2: potassium carbonate / acetone / 24 h / 20 - 50 °C

With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; potassium carbonate; triethylamine; In tetrahydrofuran; acetone;
DOI:10.1002/chem.202100143

Reference yield: 80.0%

: 1416895-64-1
4-methyl-N-(3-methyl-2-oxobutyl)-N-(3-phenylprop-2-yn-1-yl)benzenesulfonamide

: 98-80-6
phenylboronic acid

: (R)-3-isopropyl-4,5-diphenyl-1-tosyl-1,2,3,6-tetrahydropyridin-3-ol

: C₂₇H₂₉NO₃S

Guidance literature:: With nickel(II) acetate tetrahydrate; (S)-4-tert-butyl-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-1,3-oxazol; In 2,2,2-trifluoroethanol; at 20 - 80 ℃; for 24.1667h; enantioselective reaction; Sealed tube; Inert atmosphere;
DOI:10.1002/chem.202100143