(4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

Base Information

Chemical Name:(4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone
CAS No.:1364523-98-7
Molecular Formula:C₂₄H₂₅ClN₄O₃
Molecular Weight:452.941
Hs Code.:

Synonyms:(4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

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Chemical Property of (4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

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Technology Process of (4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

There total 5 articles about (4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-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: 54.0%

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

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

: 1364523-98-7
(4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

Guidance literature:: With triethylamine; HATU; at 20 ℃; for 13h;

Reference yield:

: 1364523-76-1
tert-butyl 4-(3-(tert-butoxycarbonylamino)-6-chlorophenyl)piperazine-1-carboxylate

: 1364523-98-7
(4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

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

2: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 85 °C / Inert atmosphere

3: dichloromethane / 1 h / 20 °C

4: triethylamine; HATU / 13 h / 20 °C

With potassium phosphate; N-Bromosuccinimide; triethylamine; HATU; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

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

: 1364523-98-7
(4-(5-amino-2-chloro-4-vinylphenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

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: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / 85 °C / Inert atmosphere

5.1: dichloromethane / 1 h / 20 °C

6.1: triethylamine; HATU / 13 h / 20 °C

With potassium phosphate; N-Bromosuccinimide; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; triethylamine; HATU; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium diacetate; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene;