5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Base Information

Chemical Name:5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one
CAS No.:1033443-73-0
Molecular Formula:C₂₅H₃₇N₇O
Molecular Weight:451.615
Hs Code.:

Synonyms:5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

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Chemical Property of 5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

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Technology Process of 5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

There total 5 articles about 5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-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:

: 1033443-96-7
5-chloro-1-methyl-3-propyl-1,6-dihydro-pyrazolo[4,3-d]pyrimidin-7-one

: 1033444-15-3
C₁₆H₂₇N₃

: 1033443-73-0
5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Guidance literature:: In tert-butyl alcohol; at 120 ℃; for 48h; sealed tube;

Reference yield:

: 848126-89-6
1-methyl-3-propyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-d]pyrimidin-5,7-dione

: 1033443-73-0
5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: trichlorophosphate / N,N-dimethyl-formamide / 7 - 16 h / Heating / reflux

2.1: potassium hydroxide; water / 1,4-dioxane / 1 h / 20 °C / Heating / reflux

2.2: 20 °C / pH 1

3.1: tert-butyl alcohol / 48 h / 120 °C / sealed tube

With potassium hydroxide; water; trichlorophosphate; N,N-dimethyl-formamide; In 1,4-dioxane; tert-butyl alcohol;

Reference yield:

: 139756-02-8
4-amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamide

: 1033443-73-0
5-(isobutyl(3-(4-methylpiperazin-1-yl)benzyl)amino)-1-methyl-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetonitrile / 16 h / Heating / reflux

2.1: trichlorophosphate / N,N-dimethyl-formamide / 7 - 16 h / Heating / reflux

3.1: potassium hydroxide; water / 1,4-dioxane / 1 h / 20 °C / Heating / reflux

3.2: 20 °C / pH 1

4.1: tert-butyl alcohol / 48 h / 120 °C / sealed tube

With potassium hydroxide; water; trichlorophosphate; N,N-dimethyl-formamide; In 1,4-dioxane; acetonitrile; tert-butyl alcohol;