N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

Base Information

Chemical Name:N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide
CAS No.:209115-59-3
Molecular Formula:C₂₀H₂₂N₂O₅S
Molecular Weight:402.471
Hs Code.:

Synonyms:N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

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Chemical Property of N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

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Technology Process of N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

There total 4 articles about N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-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: 75.0%

: 773-64-8
2-mesitylenesulphonyl chloride

: 157887-84-8
N-(aminooxypropyl)phthalimide

: 209115-59-3
N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; for 24h; Ambient temperature;
DOI:10.1055/s-1998-2073

Reference yield:

: 524-38-9
N-hydroxyphthalimide

: 209115-59-3
N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / DEAD, Ph₃P / tetrahydrofuran / 2 h / Ambient temperature

2: 55 percent / DBU / acetonitrile / 12 h / Ambient temperature

3: 75 percent / Et₃N / CH₂Cl₂ / 24 h / Ambient temperature

With 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1055/s-1998-2073

Reference yield:

: 524-38-9
N-hydroxyphthalimide

: 209115-59-3
N-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propoxy]-2,4,6-trimethyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: DBU / dimethylformamide / 8 h / 85 °C

2: pyridine / 8 h / 20 °C

With pyridine; 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; 1: Condensation / 2: Condensation;
DOI:10.1016/S0960-894X(00)00201-8