ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate

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Chemical Name:ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate
CAS No.:1070901-30-2
Molecular Formula:C₂₅H₂₇BrF₃N₃O₄
Molecular Weight:570.406
Hs Code.:

Synonyms:ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate

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Chemical Property of ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate

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Technology Process of ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate

There total 2 articles about ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate 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: 75.0%

: 1070901-28-8
(E)-ethyl 4-[(4-bromophenyl)(2-(tert-butylamino)-1-(2-nitro-4-(trifluoromethyl)phenyl)-2-oxoethyl)amino]-4-oxobut-2-enoate

: 1070901-30-2
ethyl (E)-4-((1-(2-amino-4-(trifluoromethyl)phenyl)-2-(tert-butylamino)-2-oxoethyl)(4-bromophenyl)amino)-4-oxobut-2-enoate

: ethyl 2-(4-(4-bromophenyl)-5-(tert-butylcarbamoyl)-3-oxo-8-(trifluoromethyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepin-2-yl)acetate

: ethyl 2-(4-(4-bromophenyl)-5-(tert-butylcarbamoyl)-3-oxo-8-(trifluoromethyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepin-2-yl)acetate

Guidance literature:: With iron; ammonium chloride; In ethanol; water; at 150 ℃; for 0.75h; under 7500.75 Torr; optical yield given as %de; chemoselective reaction; Microwave irradiation;
DOI:10.1021/ol801841m