2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

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Chemical Name:2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione
CAS No.:625123-61-7
Molecular Formula:C₃₂H₃₃N₃O₈S₂
Molecular Weight:651.761
Hs Code.:

2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[<i>de</i>]isoquinoline-1,3-dione

Synonyms:2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

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Chemical Property of 2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

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Technology Process of 2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

There total 6 articles about 2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-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: 72.0%

: 625123-60-6
2-(3-{4-[(2S,4R)-2-(Bis-ethylsulfanyl-methyl)-4-hydroxy-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

: 625123-61-7
2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

Guidance literature:: With N-methyl-2-indolinone; tetrapropylammonium perruthennate; In dichloromethane; acetonitrile; at 20 ℃; for 2.5h;
DOI:10.1016/S0960-894X(03)00718-2

Reference yield:

: 81-83-4
1,8-Naphthalimide

: 625123-61-7
2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / K₂CO₃ / dimethylformamide / 12 h / 20 °C

2: 72 percent / TPAP; NMO / CH₂Cl₂; acetonitrile / 2.5 h / 20 °C

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0960-894X(03)00718-2

Reference yield:

: (2S,4R)-1-[4-(3-Bromo-propoxy)-5-methoxy-2-nitro-benzoyl]-4-hydroxy-pyrrolidine-2-carboxylic acid methyl ester

: 625123-61-7
2-(3-{4-[2-(bis-ethylsulfanyl-methyl)-4-oxo-pyrrolidine-1-carbonyl]-2-methoxy-5-nitro-phenoxy}-propyl)-benzo[de]isoquinoline-1,3-dione

Guidance literature:: Multi-step reaction with 5 steps

1: 88 percent / imidazole / CH₂Cl₂ / 12 h / 20 °C

2: 68 percent / DIBAL-H / CH₂Cl₂ / 1 h / -78 °C

3: 85 percent / TMS-Cl / CHCl₃ / 18 h / 20 °C

4: 90 percent / K₂CO₃ / dimethylformamide / 12 h / 20 °C

5: 72 percent / TPAP; NMO / CH₂Cl₂; acetonitrile / 2.5 h / 20 °C

With 1H-imidazole; chloro-trimethyl-silane; N-methyl-2-indolinone; tetrapropylammonium perruthennate; diisobutylaluminium hydride; potassium carbonate; In dichloromethane; chloroform; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0960-894X(03)00718-2