2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

Base Information

Chemical Name:2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol
CAS No.:913652-84-3
Molecular Formula:C₂₃H₂₄ClN₃O₃
Molecular Weight:425.915
Hs Code.:

Synonyms:2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

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Chemical Property of 2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

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Technology Process of 2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

There total 7 articles about 2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol 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:

: 913651-30-6
2-((5-chloro-2-[(2-methylpropyl)oxy]phenyl)methyl)-1,3-oxazole-4-carboxylic acid

: 15788-14-4
2-(3,4-diaminophenyl)ethanol

: 913652-84-3
2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

Guidance literature:: 2-((5-chloro-2-[(2-methylpropyl)oxy]phenyl)methyl)-1,3-oxazole-4-carboxylic acid; 2-(3,4-diaminophenyl)ethanol; With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 3h;

With acetic acid; at 110 ℃; for 0.5h;

Reference yield:

: 26938-87-4
(5-chloro-2-((2-methylpropyl)oxy)phenyl)acetonitrile

: 913652-84-3
2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / 2.5 h / 0 - 20 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

3.1: hexamethylenetetramine; 1,8-diazabicyclo[5.4.0]undec-7-ene; copper(ll) bromide / dichloromethane / 0 - 20 °C

4.1: sodium hydroxide; water / methanol / 1 h / 50 °C

5.1: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 20 °C

5.2: 0.5 h / 110 °C

With 4-methyl-morpholine; hydrogenchloride; sodium hydroxide; hexamethylenetetramine; water; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; copper(ll) bromide; In methanol; dichloromethane;

Reference yield:

: 4-chloro-2-(chloromethyl)phenyl 2-methylpropyl ether

: 913652-84-3
2-(2-(2-({5-chloro-2-[(2-methylpropyl)oxy]phenyl}methyl)-1,3-oxazol-4-yl)-3H-benzimidazol-5-yl)ethanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: dimethyl sulfoxide / 1.67 h / 60 °C

2.1: hydrogenchloride / 2.5 h / 0 - 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C

4.1: hexamethylenetetramine; 1,8-diazabicyclo[5.4.0]undec-7-ene; copper(ll) bromide / dichloromethane / 0 - 20 °C

5.1: sodium hydroxide; water / methanol / 1 h / 50 °C

6.1: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 20 °C

6.2: 0.5 h / 110 °C

With 4-methyl-morpholine; hydrogenchloride; sodium hydroxide; hexamethylenetetramine; water; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; copper(ll) bromide; In methanol; dichloromethane; dimethyl sulfoxide;