5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

Base Information

Chemical Name:5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one
CAS No.:1354030-44-6
Molecular Formula:C₂₁H₂₄Cl₂N₄O₂
Molecular Weight:435.353
Hs Code.:

Synonyms:5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

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Chemical Property of 5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

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Technology Process of 5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

There total 6 articles about 5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-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: 32.0%

: 1354030-43-5
5-(3-bromopropoxy)-1H-benzo[d]imidazol-2(3H)-one

: 839712-09-3
1-(2,3-dichlorophenyl)-1,4-diazepane hydrochloride

: 1354030-44-6
5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: 5-(3-bromopropoxy)-1H-benzo[d]imidazol-2(3H)-one; With sodium iodide; In acetonitrile; for 0.5h; Reflux;

1-(2,3-dichlorophenyl)-1,4-diazepane hydrochloride; With potassium carbonate; In acetonitrile; for 6h; Reflux;

Reference yield:

: 96-96-8
4-methoxy-2-nitroaniline

: 1354030-44-6
5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: ammonium chloride; iron / ethanol; water / Reflux

2.1: iodine / methanol / 1 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 130 °C

4.1: hydrogen iodide / 12 h / 130 °C

4.2: pH 12

5.1: potassium carbonate / ethanol / Reflux

6.1: sodium iodide / acetonitrile / 0.5 h / Reflux

6.2: 6 h / Reflux

With hydrogen iodide; iodine; iron; potassium carbonate; ammonium chloride; sodium iodide; In methanol; ethanol; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 213118-56-0
(2-amino-4-methoxyphenyl)carbamate tert-butyl ester

: 1354030-44-6
5-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 130 °C

2.1: hydrogen iodide / 12 h / 130 °C

2.2: pH 12

3.1: potassium carbonate / ethanol / Reflux

4.1: sodium iodide / acetonitrile / 0.5 h / Reflux

4.2: 6 h / Reflux

With hydrogen iodide; potassium carbonate; sodium iodide; In ethanol; N,N-dimethyl-formamide; acetonitrile;