6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

Base Information

Chemical Name:6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one
CAS No.:88968-21-2
Molecular Formula:C₂₃H₂₁ClN₆O₄
Molecular Weight:480.911
Hs Code.:

Synonyms:6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

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Chemical Property of 6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

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Technology Process of 6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

There total 9 articles about 6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-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: 67.0%

: 101928-18-1
6-o-chlorophenyl-2,4-dihydro-2(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one 5-oxide

: 88968-21-2
6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

Guidance literature:: With trifluoroacetic anhydride; In dichloromethane; for 0.25h; Heating;

Reference yield:

: 109-01-3
1-methyl-piperazine

: 88968-21-2
6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / toluene / 9 h / Heating

2: 67 percent / trifluoroacetic anhydride / CH₂Cl₂ / 0.25 h / Heating

With trifluoroacetic anhydride; In dichloromethane; toluene;

Reference yield:

: 2011-66-7
2'-chloro-5-nitro-2-aminobenzophenone

: 88968-21-2
6-o-chlorophenyl-2,4-dihydro-4-hydroxy-2-(4-methyl-1-piperazinyl)methylene-8-nitro-1H-imidazo<1,2-a><1,4>benzodiazepin-1-one

Guidance literature:: Multi-step reaction with 8 steps

1: 59 percent / NH₂OH, 2 N HCl / ethanol; H₂O / 1.) 2 h; 2.) 2.5 h, reflux

2: 75 percent / MnO₂ / CH₂Cl₂ / 20 h / Ambient temperature

3: 80 percent / methanol / 2 h / Ambient temperature

4: 90 percent / imidazole / 48 h / Heating

5: 55 percent / 2 N NaOH / dimethylformamide / 5 °C

6: 1.) dicyclohexylcarbodiimide; 2.) triethylamine / 1.) CH₂Cl₂, 1 h, RT; 2.) 2 h

7: 70 percent / toluene / 9 h / Heating

8: 67 percent / trifluoroacetic anhydride / CH₂Cl₂ / 0.25 h / Heating

With 1H-imidazole; hydrogenchloride; manganese(IV) oxide; sodium hydroxide; hydroxylamine; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic anhydride; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;