2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

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Chemical Name:2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile
CAS No.:1364523-88-5
Molecular Formula:C₂₃H₂₂ClN₅O₃
Molecular Weight:451.912
Hs Code.:

Synonyms:2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

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Chemical Property of 2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

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Technology Process of 2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

There total 6 articles about 2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile 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: 52.0%

: 2-amino-5-chloro-4-(piperazin-1-yl)benzonitrile ditrifluoroacetate

: 93041-44-2
3-(2-methoxyphenyl)-5-methylisoxazole-4-carboxylic acid

: 1364523-88-5
2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃;

Reference yield:

: 823-54-1
3-bromo-4-chloroaniline

: 1364523-88-5
2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / dichloromethane / 0 °C

1.2: 20 °C

2.1: caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / palladium diacetate / toluene / 110 °C

3.1: N-Bromosuccinimide / dichloromethane; methanol / 1 h / 20 °C

4.1: 1,1'-bis-(diphenylphosphino)ferrocene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 120 °C / Inert atmosphere

5.1: dichloromethane / 1 h / 20 °C

6.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With dmap; 1,1'-bis-(diphenylphosphino)ferrocene; N-Bromosuccinimide; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; In methanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1080573-26-7
tert-butyl N-(3-bromo-4-chloro-phenyl)carbamate

: 1364523-88-5
2-amino-5-chloro-4-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / palladium diacetate / toluene / 110 °C

2: N-Bromosuccinimide / dichloromethane; methanol / 1 h / 20 °C

3: 1,1'-bis-(diphenylphosphino)ferrocene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 120 °C / Inert atmosphere

4: dichloromethane / 1 h / 20 °C

5: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 °C

With dmap; 1,1'-bis-(diphenylphosphino)ferrocene; N-Bromosuccinimide; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; In methanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;