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

Base Information

Chemical Name:(4-(5-amino-2-chloro-4-nitrophenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone
CAS No.:1364523-75-0
Molecular Formula:C₂₂H₂₂ClN₅O₅
Molecular Weight:471.9
Hs Code.:

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

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

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

There total 1 articles about (4-(5-amino-2-chloro-4-nitrophenyl)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: 38.9%

: 4-chloro-2-nitro-5-(piperazin-1-yl)aniline

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

: 1364523-75-0
(4-(5-amino-2-chloro-4-nitrophenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; N,N-dimethyl-formamide;

Reference yield: 74.9%

: 1364523-75-0
(4-(5-amino-2-chloro-4-nitrophenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

: 100-07-2
4-methoxy-benzoyl chloride

: 1364522-06-4
N-(4-chloro-5-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)-2-nitrophenyl)-4-methoxybenzamide

Guidance literature:: (4-(5-amino-2-chloro-4-nitrophenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone; 4-methoxy-benzoyl chloride; With dmap; 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine; In 1,2-dichloro-ethane; at 80 ℃; for 3h;

With piperidine; In 1,2-dichloro-ethane; at 20 ℃; for 1h;

Reference yield: 64.4%

: 876-08-4
p-(chloromethyl)benzoyl chloride

: 1364523-75-0
(4-(5-amino-2-chloro-4-nitrophenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone

: 124-40-3
dimethyl amine

: 76-05-1
trifluoroacetic acid

: N-(4-chloro-5-(4-(3-(2-methoxyphenyl)-5-methylisoxazole-4-carbonyl)piperazin-1-yl)-2-nitrophenyl)-4-((dimethylamino)methyl)benzamide trifluoroacetate

Guidance literature:: p-(chloromethyl)benzoyl chloride; (4-(5-amino-2-chloro-4-nitrophenyl)piperazin-1-yl)(3-(2-methoxyphenyl)-5-methylisoxazol-4-yl)methanone; With dmap; 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine; In 1,2-dichloro-ethane; for 4h; Heating;

dimethyl amine; In water; 1,2-dichloro-ethane; at 20 ℃; for 3h;

trifluoroacetic acid;