(4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

Base Information

Chemical Name:(4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone
CAS No.:1362020-52-7
Molecular Formula:C₂₂H₂₃ClN₆O₄
Molecular Weight:470.915
Hs Code.:

Synonyms:(4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

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Chemical Property of (4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

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Technology Process of (4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

There total 4 articles about (4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone 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: 74.5%

: 1362020-68-5
C₁₁H₁₁N₃O₃

: 114878-60-3
1-(2-chloro-4-nitro-phenyl)piperazine

: 1362020-52-7
(4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

Guidance literature:: C₁₁H₁₁N₃O₃; With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 2h;

1-(2-chloro-4-nitro-phenyl)piperazine; With triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 3h; Cooling with ice;
DOI:10.1021/jm2013503

Reference yield:

: 90-04-0
2-methoxy-phenylamine

: 1362020-52-7
(4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / water; ethyl acetate / 0.17 h / 0 °C

1.2: 0.5 h

1.3: 0.5 h / 0 °C

2.1: toluene / 120 °C

3.1: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C

4.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 2 h / 20 °C

4.2: 3 h / 20 °C / Cooling with ice

With hydrogenchloride; oxalyl dichloride; water; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm2013503

Reference yield:

: 1362020-54-9
C₁₃H₁₅N₃O₃

: 1362020-52-7
(4-(2-chloro-4-nitrophenyl)-1,4-diazepan-1-yl)(1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazol-5-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C

2.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 2 h / 20 °C

2.2: 3 h / 20 °C / Cooling with ice

With oxalyl dichloride; water; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm2013503