5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

Base Information

Chemical Name:5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one
CAS No.:1374262-96-0
Molecular Formula:C₂₂H₁₉N₃O₂
Molecular Weight:357.412
Hs Code.:

Synonyms:5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

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Chemical Property of 5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

Chemical Property:

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Technology Process of 5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

There total 1 articles about 5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one 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:

: 31984-10-8
1-bromo-4-phenylbutan-2-one

: 885-70-1
5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

: 1374262-96-0
5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

Guidance literature:: 5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one; With sodium hydride; In ISOPROPYLAMIDE; mineral oil; at 0 - 20 ℃;

1-bromo-4-phenylbutan-2-one; In ISOPROPYLAMIDE; mineral oil; at 0 - 20 ℃; for 2h;

Reference yield:

: 1374262-96-0
5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

: 1374262-97-1
2-phenethyl-9H-benzo[f]imidazo[1,2-d]pyrido[2,3-b][1,4]diazepine

Guidance literature:: With ammonium acetate; acetic acid; at 120 ℃; for 8h;

Reference yield:

: 1374262-96-0
5-(2-oxo-4-phenylbutyl)-5H-benzo[e]pyrido[3,2-b][1,4]diazepin-6(11H)-one

: 1374262-99-3
tert-butyl (1-(4-(2-phenethyl-9H-benzo[f]imidazo[1,2-d]pyrido[2,3-b][1,4]diazepin-3-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: ammonium acetate; acetic acid / 8 h / 120 °C

2: N-Bromosuccinimide / tetrahydrofuran / 0.5 h / 20 °C

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium hydrogencarbonate / ethanol; water; toluene / 100 °C / Inert atmosphere

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; ammonium acetate; sodium hydrogencarbonate; acetic acid; In tetrahydrofuran; ethanol; water; toluene;