4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

Base Information

Chemical Name:4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione
CAS No.:907198-49-6
Molecular Formula:C₂₉H₂₇Cl₂IN₄O₅
Molecular Weight:709.368
Hs Code.:

4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1<i>H</i>-benzo[<i>e</i>][1,4]diazepine-2,5-dione

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Chemical Property of 4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

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Technology Process of 4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

There total 7 articles about 4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-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:

: 787633-79-8
(R,S)-1-(4-chloro-2-nitrophenyl)ethanol

: 907198-49-6
4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

Guidance literature:: Multi-step reaction with 7 steps

1: NEt₃ / CH₂Cl₂ / 16 h

2: 93 percent / LiOH / methanol; H₂O / 16 h

3: 87 percent / Ph₃P; DIAD / tetrahydrofuran / 3 h / 20 °C

4: 96 percent / hydrazine / tetrahydrofuran / 1 h / 80 °C

5: methanol / 48 h / 20 °C

6: AcCl; MeOH / 1 h / 20 - 60 °C

7: Bu₄NI; K₂CO₃ / tetrahydrofuran / 80 °C

With methanol; lithium hydroxide; di-isopropyl azodicarboxylate; tetra-(n-butyl)ammonium iodide; potassium carbonate; triethylamine; acetyl chloride; triphenylphosphine; hydrazine; In tetrahydrofuran; methanol; dichloromethane; water; 3: Mitsunobu reaction / 5: Ugi reaction;
DOI:10.1016/j.bmcl.2006.03.067

Reference yield:

: 898222-44-1
(R)-1-(4-Chloro-2-nitro-phenyl)-ethylamine

: 907198-49-6
4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / 48 h / 20 °C

2: AcCl; MeOH / 1 h / 20 - 60 °C

3: Bu₄NI; K₂CO₃ / tetrahydrofuran / 80 °C

With methanol; tetra-(n-butyl)ammonium iodide; potassium carbonate; acetyl chloride; In tetrahydrofuran; methanol; 1: Ugi reaction;
DOI:10.1016/j.bmcl.2006.03.067

Reference yield:

: 898222-42-9
(S)-1-(4-Chloro-2-nitro-phenyl)-ethanol

: 907198-49-6
4-[1-(4-chloro-2-nitro-phenyl)-ethyl]-3-(4-chloro-phenyl)-7-iodo-1-(2-morpholin-4-yl-ethyl)-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / Ph₃P; DIAD / tetrahydrofuran / 3 h / 20 °C

2: 96 percent / hydrazine / tetrahydrofuran / 1 h / 80 °C

3: methanol / 48 h / 20 °C

4: AcCl; MeOH / 1 h / 20 - 60 °C

5: Bu₄NI; K₂CO₃ / tetrahydrofuran / 80 °C

With methanol; di-isopropyl azodicarboxylate; tetra-(n-butyl)ammonium iodide; potassium carbonate; acetyl chloride; triphenylphosphine; hydrazine; In tetrahydrofuran; methanol; 1: Mitsunobu reaction / 3: Ugi reaction;
DOI:10.1016/j.bmcl.2006.03.067