tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

Base Information

Chemical Name:tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate
CAS No.:1085941-17-8
Molecular Formula:C₃₀H₃₈N₄O₃
Molecular Weight:502.657
Hs Code.:

Synonyms:tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

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Chemical Property of tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

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Technology Process of tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

There total 6 articles about tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate 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:

: 30414-55-2
methyl 5-methyl-3-oxohexanoate

: 1085941-17-8
tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium methylate / methanol / 20 °C

2: N-iodo-succinimide / dichloromethane; acetonitrile / 80 °C

3: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / N,N-dimethyl-formamide / 60 °C

4: N-Bromosuccinimide; trifluoroacetic acid / dichloromethane; acetonitrile / 3 h / 20 °C

5: 1 h / 70 °C

With potassium phosphate; N-Bromosuccinimide; N-iodo-succinimide; sodium methylate; trifluoroacetic acid; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1085941-16-7
3-benzyl-2-(1-bromo-2-methylpropyl)pyrimido[2,1-a]isoindol-4-(6H)-one

: 75178-96-0
N-Boc-1,3-diaminopropane

: 1085941-17-8
tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

Guidance literature:: at 70 ℃; for 1h;

Reference yield:

: 1085941-12-3
2-isobutylpyrimido[2,1-a]isoindol-4(6H)-one

: 1085941-17-8
tert-butyl 3-(1-(3-benzyl-4-oxo-4,6-dihydropyrimido[2,1-a]isoindol-2-yl)-2-methylpropylamino)propylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1: N-iodo-succinimide / dichloromethane; acetonitrile / 80 °C

2: potassium phosphate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / N,N-dimethyl-formamide / 60 °C

3: N-Bromosuccinimide; trifluoroacetic acid / dichloromethane; acetonitrile / 3 h / 20 °C

4: 1 h / 70 °C

With potassium phosphate; N-Bromosuccinimide; N-iodo-succinimide; trifluoroacetic acid; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;