(2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

Base Information

Chemical Name:(2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester
CAS No.:119487-35-3
Molecular Formula:C₃₀H₃₁N₅O₄
Molecular Weight:525.607
Hs Code.:

Synonyms:(2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

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Chemical Property of (2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

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Technology Process of (2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

There total 5 articles about (2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester 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:

: 108895-98-3
benzyl 2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-ylcarbamate

: 119487-35-3
(2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, 0 deg C, 2 h, 2.) DMF, from 0 deg C to RT, 1 h

2: 93 percent / 1N aq. NaOH / tetrahydrofuran / 3 h / 23 °C

3: 96 percent / SOCl₂ / toluene / 1 h / 90 °C

4: tetrahydrofuran / 1 h / 23 °C

With sodium hydroxide; thionyl chloride; sodium hydride; In tetrahydrofuran; toluene;
DOI:10.1021/jm00078a018

Reference yield:

: 172968-04-6
1(Carboxymethyl)-1,3-Dihydro-5-phenyl-3(R,S)-[(benzyloxycarbonyl)-amino]2H-1,4-benzodiazepin-2-one

: 119487-35-3
(2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / SOCl₂ / toluene / 1 h / 90 °C

2: tetrahydrofuran / 1 h / 23 °C

With thionyl chloride; In tetrahydrofuran; toluene;
DOI:10.1021/jm00078a018

Reference yield:

: 119487-58-0
ethyl 3-<(benzyloxycarbonyl)amino>-2,3-dihydro-2-oxo-5-phenyl-1H-1,4-benzodiazepine-1-acetate

: 119487-35-3
(2,3-Dihydro-1-(2-(4-methyl-1-piperazinyl)-2-oxoethyl)-2-oxo-5-phenyl-1H-1,4-benzodiazepin-3-yl)-carbamic acid phenylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / 1N aq. NaOH / tetrahydrofuran / 3 h / 23 °C

2: 96 percent / SOCl₂ / toluene / 1 h / 90 °C

3: tetrahydrofuran / 1 h / 23 °C

With sodium hydroxide; thionyl chloride; In tetrahydrofuran; toluene;
DOI:10.1021/jm00078a018