3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

Base Information

Chemical Name:3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione
CAS No.:930591-53-0
Molecular Formula:C₁₉H₁₉N₃O₃
Molecular Weight:337.378
Hs Code.:

Synonyms:3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

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Chemical Property of 3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

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Technology Process of 3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

There total 7 articles about 3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione 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: 23.0%

: 930591-54-1
1-Acetyl-3-{(Z)-1-[5-(tert-Butyl)-4-oxazolyl]methylidene}-2,5-piperazinedione

: 100-52-7
benzaldehyde

: 930591-53-0
3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 85 ℃; for 3h; Product distribution / selectivity;

Reference yield: 23.0%

: 930591-53-0
3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

Guidance literature:

Reference yield:

: 1538-75-6
2,2-dimethylpropanoic anhydride

: 930591-53-0
3-{(Z)-1-[5-(tert-butyl)-1H-4-oxazolyl]methylidene}-6-[(Z)-1-(phenyl)methylidene]-2,5-piperazinedione

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 4 - 20 °C

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / -60 - -40 °C

2.2: -60 °C

3.1: manganese(IV) oxide / acetone / 20 °C

4.1: caesium carbonate / N,N-dimethyl-formamide / 6 h / 20 - 45 °C

5.1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 85 °C

With manganese(IV) oxide; lithium aluminium tetrahydride; caesium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; N,N-dimethyl-formamide; acetone;