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1056624-11-3

Basic Information
CAS No.: 1056624-11-3
Name: 2-(4-(piperazin-1-yl)phenyl)pyrimidine hydrochloride
Article Data: 3
Molecular Structure:
Molecular Structure of 1056624-11-3 (2-(4-(piperazin-1-yl)phenyl)pyrimidine hydrochloride)
Formula: C14H16N4.ClH
Molecular Weight: 276.769
Synonyms: 2,4,6,8-Tetrahydroxy-pyrimido[5,4-d]pyrimidine
Appearance: Yellow power
PSA: 41.05000
LogP: 2.74900
Synthetic route
942189-35-7

4-(4-pyrimidin-2-yl-phenyl)-piperazine-1-carboxylic acid tert-butyl ester

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In 1,4-dioxane; dichloromethane
With hydrogenchloride In 1,4-dioxane; dichloromethane for 2h;
With hydrogenchloride In 1,4-dioxane; dichloromethane for 2h;

C21H35BN2O4

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: ammonium chloride / tetrahydrofuran; hexanes; water / 0.08 h
1.2: 1 h
2.1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; N,N-dimethyl-formamide / 8 h / 80 °C
3.1: hydrogenchloride / 1,4-dioxane; dichloromethane / 2 h
View Scheme
352437-09-3

tert-butyl 4-(4-bromophenyl)piperazine-1-carboxylate

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1.1: n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C
1.2: 18.17 h / 20 °C
2.1: ammonium chloride / tetrahydrofuran; hexanes; water / 0.08 h
2.2: 1 h
3.1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; N,N-dimethyl-formamide / 8 h / 80 °C
4.1: hydrogenchloride / 1,4-dioxane; dichloromethane / 2 h
View Scheme
457613-78-4

4-(4-(tert-butoxycarbonyl)piperazin-1-yl)phenylboronic acid

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; N,N-dimethyl-formamide / 8 h / 80 °C
2: hydrogenchloride / 1,4-dioxane; dichloromethane / 2 h
View Scheme

1-(4-Bromophenyl)Piperazine Monohydrochloride

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: triethylamine / dichloromethane / 1 h
2.1: n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C
2.2: 18.17 h / 20 °C
3.1: ammonium chloride / tetrahydrofuran; hexanes; water / 0.08 h
3.2: 1 h
4.1: potassium carbonate / bis-triphenylphosphine-palladium(II) chloride / water; N,N-dimethyl-formamide / 8 h / 80 °C
5.1: hydrogenchloride / 1,4-dioxane; dichloromethane / 2 h
View Scheme
942189-34-6

1-carboxymethyl-pyrrolidine-3-carboxylic acid methyl ester

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

942189-36-8

1-{2-oxo-2-[4-(4-pyrimidin-2-yl-phenyl)-piperazin-1-yl]-ethyl}-pyrrolidine-3-carboxylic acid methyl ester

Conditions
ConditionsYield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide for 24h;
1056623-86-9

1-tert-butoxycarbonylmethyl-3-methoxymethyl-pyrrolidine-3-carboxylic acid methyl ester

1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

942189-79-9

3-methoxymethyl-1-{2-oxo-2-[4-(4-pyrimidin-2-yl-phenyl)-piperazin-1-yl]-ethyl}-pyrrolidine-3-carboxylic acid methyl ester

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; HATU In 1,2-dimethoxyethane for 4h;
1056624-11-3

2-(4-piperazin-1-yl-phenyl)-pyrimidine hydrochloride

79-04-9

chloroacetyl chloride

2-chloro-1-[4-(4-pyrimidin-2-yl-phenyl)-3,6-dihydro-2H-pyridin-1-yl]-ethanone

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; for 0.5h;
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