N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

Base Information

Chemical Name:N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide
CAS No.:857886-97-6
Molecular Formula:C₂₃H₂₆Cl₂N₂O₄S
Molecular Weight:497.442
Hs Code.:

<i>N</i>-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-<i>N</i>-(4-methyl-2-oxo-2<i>H</i>-chromen-7-yl)-benzenesulfonamide

Synonyms:N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

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Chemical Property of N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

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Technology Process of N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

There total 3 articles about N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-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: 80.0%

: 817-09-4
tris-(2-chloroethyl)amine hydrochloride

: 101973-09-5
7-[N-(p-toluenesulfonyl)amino]-4-methylcoumarin

: 857886-97-6
N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

Guidance literature:: With caesium carbonate; In acetonitrile; at 80 ℃; for 18h;
DOI:10.1016/j.tetlet.2005.04.059

Reference yield:

: 26093-31-2
7-amino-4-methylcoumarin.

: 857886-97-6
N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / pyridine / CH₂Cl₂ / 18 h / 20 °C

2: 80 percent / Cs₂CO₃ / acetonitrile / 18 h / 80 °C

With pyridine; caesium carbonate; In dichloromethane; acetonitrile;
DOI:10.1016/j.tetlet.2005.04.059

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 857886-97-6
N-{2-[bis-(2-chloro-ethyl)-amino]-ethyl}-4-methyl-N-(4-methyl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / pyridine / CH₂Cl₂ / 18 h / 20 °C

2: 80 percent / Cs₂CO₃ / acetonitrile / 18 h / 80 °C

With pyridine; caesium carbonate; In dichloromethane; acetonitrile;
DOI:10.1016/j.tetlet.2005.04.059