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53617-36-0

Basic Information
CAS No.: 53617-36-0
Name: 1-METHYL-4-(PIPERIDIN-4-YL)-PIPERAZINE
Article Data: 6
Molecular Structure:
Molecular Structure of 53617-36-0 (1-METHYL-4-(PIPERIDIN-4-YL)-PIPERAZINE)
Formula: C10H21N3
Molecular Weight: 183.297
Synonyms: 1-Methyl-4-(4-piperidinyl)piperazine;1-Methyl-4-(piperidin-4-yl)piperazine;(1-methyl-4-piperidin-4-yl)-piperazine;
Density: 0.992g/cm3
Melting Point: 53-56oC
Boiling Point: 260.9oC at 760 mmHg
Flash Point: 113.8oC
Solubility: Soluble in water.
Hazard Symbols: Xi
PSA: 18.51000
LogP: 0.19040
Synthetic route

1-(1-benzylpiperidin-4-yl)-4-methylpiperazine

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

Conditions
ConditionsYield
100%
With palladium on activated charcoal; hydrogen In methanol at 20℃; under 3750.38 Torr; for 2h;74.9%
109-01-3

1-methyl-piperazine

79099-07-3

N-tert-butyloxycarbonylpiperidin-4-one

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane at 0 - 20℃; for 16h;60%
Stage #1: 1-methyl-piperazine; N-tert-butyloxycarbonylpiperidin-4-one With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane at 0 - 20℃; for 16h;
Stage #2: With hydrogenchloride In methanol at 40℃; for 12h;
60%
Multi-step reaction with 2 steps
1: acetic acid; sodium tris(acetoxy)borohydride / ethanol / 12 h / 20 °C
2: hydrogenchloride / methanol / 12 h / 0 °C
View Scheme
79099-07-3

N-tert-butyloxycarbonylpiperidin-4-one

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 0 - 20 °C
2: hydrogenchloride / methanol / 12 h / 40 °C
View Scheme

tert-butyl 4-(4-methylpiperazin-1-yl)piperidine-1-carboxylate

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

Conditions
ConditionsYield
With hydrogenchloride In methanol at 40℃; for 12h;0.826 g
With hydrogenchloride In methanol at 0℃; for 12h;
109-01-3

1-methyl-piperazine

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 16 h / 0 - 20 °C
2: hydrogenchloride / methanol / 12 h / 40 °C
View Scheme
Multi-step reaction with 2 steps
1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 3 h / 20 °C
2: palladium on activated charcoal; hydrogen / methanol / 2 h / 20 °C / 3750.38 Torr
View Scheme
3612-20-2

1-phenylmethyl-4-piperidone

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 3 h / 20 °C
2: palladium on activated charcoal; hydrogen / methanol / 2 h / 20 °C / 3750.38 Torr
View Scheme
866087-58-3

4-(2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-piperidine-1-carboxylic acid (R)-1-carboxy-2-[3,5-dibromo-4-hydroxy-phenyl]-ethyl ester

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylic acid (R)-1-(3,5-dibromo-4-hydroxy-benzyl)-2-[4-(4-methyl-piperazin-1-yl)-piperidin-1-yl]-2-oxo-ethyl ester

Conditions
ConditionsYield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 3h;99%
5081-36-7

3-methoxy-4-nitrobenzoic acid

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

(3-methoxy-4-nitrophenyl)(4-(4-methylpiperazin-1-yl)piperidin-1-yl)methanone

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃;98%
53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

868706-61-0

4-(2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-piperidine-1-carboxylic acid (R)-1-(4-amino-3-methyl-5-nitro-benzyl)-2-[4-(4-methyl-piperazin-1-yl)piperidin-1-yl]-2-oxo-ethyl ester

Conditions
ConditionsYield
Stage #1: 4-(2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-piperidine-1-carboxylic acid (R)-2-(4-amino-3-methyl-5-nitro-phenyl)-1-carboxy-ethyl ester With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; DMF (N,N-dimethyl-formamide) at 20℃; for 1h;
Stage #2: 1-methyl-4-(piperidin-4-yl)piperazine In tetrahydrofuran; DMF (N,N-dimethyl-formamide) at 20℃; for 4h;
Stage #3: With sodium hydrogencarbonate In tetrahydrofuran; DMF (N,N-dimethyl-formamide); water
97%
Stage #1: 4-(2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-piperidine-1-carboxylic acid (R)-2-(4-amino-3-methyl-5-nitro-phenyl)-1-carboxy-ethyl ester With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; DMF (N,N-dimethyl-formamide) at 20℃; for 1h;
Stage #2: 1-methyl-4-(piperidin-4-yl)piperazine In tetrahydrofuran; DMF (N,N-dimethyl-formamide) at 20℃; for 4h;
97%
686297-85-8

(R)-2-tert-butoxycarbonylamino-3-(3,4-diethyl-phenyl)-propionic acid

53617-36-0

1-methyl-4-(piperidin-4-yl)piperazine

686297-90-5

{(R)-1-(3,4-diethyl-benzyl)-2-[4-(4-methyl-piperazin-1-yl)-piperidin-1-yl]-2-oxo-ethyl}-carbamic acid tert-butylester

Conditions
ConditionsYield
With benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃;97%
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