(E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile

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Chemical Name:(E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile
CAS No.:1396320-25-4
Molecular Formula:C₂₈H₂₂N₁₀O₄S₂
Molecular Weight:626.679
Hs Code.:

Synonyms:(E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile

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Chemical Property of (E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile

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Technology Process of (E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile

There total 2 articles about (E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile 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: 69.0%

: 110-85-0
piperazine

: 1292289-98-5
C₁₂H₆N₄O₂S

: 1396320-25-4
(E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile

Guidance literature:: With dimedone; In ethanol; at 130 ℃; for 0.5h; Microwave irradiation;
DOI:10.1002/cjoc.201100719

Reference yield:

: 6097-22-9
1-(3-nitrophenyl)-2-thiocyanatoethanone

: 1396320-25-4
(E)-3-amino-3-(4-{(E)-1-amino-2-cyano-2-[4-(3-nitrophenyl)thiazol-2-yl]vinyl}piperazin-1-yl)-2-[4-(3-nitrophenyl)thiazol-2-yl]acrylonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / ethanol; water / 2 h / 20 °C

2: dimedone / ethanol / 0.5 h / 130 °C / Microwave irradiation

With dimedone; potassium hydroxide; In ethanol; water;
DOI:10.1002/cjoc.201100719