2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

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Chemical Name:2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione
CAS No.:1321626-15-6
Molecular Formula:C₂₃H₂₀N₂O₄S
Molecular Weight:420.489
Hs Code.:

Synonyms:2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

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Chemical Property of 2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

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Technology Process of 2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

There total 4 articles about 2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione 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: 61.0%

: 123-75-1
pyrrolidine

: 1321626-12-3
4-[(1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)methyl]benzenesulphonyl chloride

: 1321626-15-6
2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

Guidance literature:: at 0 - 20 ℃;
DOI:10.1016/j.bmc.2011.05.056

Reference yield:

: 81-84-5
1,8-Naphthalic anhydride

: 1321626-15-6
2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 6 h / Reflux

2: chlorosulfonic acid / 50 °C / Cooling

3: 0 - 20 °C

With chlorosulfonic acid; In ethanol;
DOI:10.1016/j.bmc.2011.05.056

Reference yield:

: 100-46-9
benzylamine

: 1321626-15-6
2-[4-(pyrrolidin-1-ylsulphonyl)benzyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 6 h / Reflux

2: chlorosulfonic acid / 50 °C / Cooling

3: 0 - 20 °C

With chlorosulfonic acid; In ethanol;
DOI:10.1016/j.bmc.2011.05.056