(Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

Base Information

Chemical Name:(Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one
CAS No.:1539318-35-8
Molecular Formula:C₁₃H₁₃F₂N₃O₂
Molecular Weight:281.262
Hs Code.:

Synonyms:(Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

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Technology Process of (Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

There total 3 articles about (Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one 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: 87.0%

: 1609105-69-2
C₁₈H₂₁F₂N₃O₄

: 1539318-35-8
(Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 25 ℃; for 2h;
DOI:10.1021/ja410819x

Reference yield:

: 1332478-75-7
(Z)-2,6-difluoro-4-((2-methyl-5-oxooxazol-4(5H)-ylidene)methyl)phenyl acetate

: 1539318-35-8
(Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / ethanol / 4 h / Reflux

2: trifluoroacetic acid / dichloromethane / 2 h / 25 °C

With potassium carbonate; trifluoroacetic acid; In ethanol; dichloromethane;
DOI:10.1021/ja410819x

Reference yield:

: 118276-06-5
3,5-difluoro-4-hydroxybenzaldehyde

: 1539318-35-8
(Z)-1-(2-aminoethyl)-4-(3,5-difluoro-4-hydroxybenzylidene)-2-methyl-1Himidazol-5(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium acetate / 1 h / 100 °C

2: potassium carbonate / ethanol / 4 h / Reflux

3: trifluoroacetic acid / dichloromethane / 2 h / 25 °C

With sodium acetate; potassium carbonate; trifluoroacetic acid; In ethanol; dichloromethane;
DOI:10.1021/ja410819x