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169447-70-5

169447-70-5 Structure

169447-70-5 Structure
IdentificationMore
[Name]

(S)-1-N-Boc-2-methylpiperazine
[CAS]

169447-70-5
[Synonyms]

(R)-1-N-BOC-2-METHYL PIPERAZINE
(R)-2-METHYL-1-BOC-PIPERAZINE
(R)-2-METHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(R)-TERT-BUTYL 2-METHYLPIPERAZINE-1-CARBOXYLATE
(S)-1-N-BOC-2-METHYL PIPERAZINE
(S)-2-METHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(S)-TERT-BUTYL 2-METHYLPIPERAZINE-1-CARBOXYLATE
(S)-1-Boc-2-methyl-piperazine
Tert-Butyl2(S)-methylpiperazine-1-carboxylate
2-S-Methyl-piperazine-1-carboxylic acid tert-butyl ester
(S)-1-N-Boc-2-Methylpiperizine tert-butyl 2(S)-methylpiperazine-1-carboxylate
(S)-N1-BOC-2-METHYLPIPERAZINE
(S)-1-Boc-2-methl-piperazine
[Molecular Formula]

C10H20N2O2
[MDL Number]

MFCD01862120
[Molecular Weight]

200.28
[MOL File]

169447-70-5.mol
Chemical PropertiesBack Directory
[Melting point ]

43.0 to 47.0 °C
[Boiling point ]

268.7±15.0 °C(Predicted)
[density ]

0.997±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

8.49±0.40(Predicted)
[color ]

White to Almost white
[Optical Rotation]

Consistent with structure
[InChI]

InChI=1S/C10H20N2O2/c1-8-7-11-5-6-12(8)9(13)14-10(2,3)4/h8,11H,5-7H2,1-4H3/t8-/m0/s1
[InChIKey]

DATRVIMZZZVHMP-QMMMGPOBSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCNC[C@@H]1C
[CAS DataBase Reference]

169447-70-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P260-P271
[RIDADR ]

UN3077
[HS Code ]

2933599590
Hazard InformationBack Directory
[Uses]

(S)-1-N-Boc-2-methylpiperazine is used in the preparation of pyrazolo[3,4-b]pyridine dual pharmacophores as PDE4-muscarinic antagonists.
[Synthesis]

A solution of (S)-2-methyl piperazine (2 g, 20 mmol) in THF (200 ml_) was mixed with nBuLi (25 ml, 1.6 M in hexanes, 40 mmol) at rt. The solution was stirred for 30 minutes before TBDMSCI (3.04 g, 20 mmol) was added. The mixture was stirred for 1 hour and then (Boc)2O (5.2 g, 24 mmol) was added to the solution. After 1 hour, the solution was diluted with H2O (50 ml). The organic layer was separated, washed with brine (50 mL), dried over Na2SO4, and concentrated EPO under vacuum. Finally, (S)-1-N-Boc-2-methylpiperazine was obtained after purification.(S)-1-N-Boc-2-methylpiperazine
[References]

[1] Patent: WO2006/55553, 2006, A2. Location in patent: Page/Page column 36; 37
[2] Journal of Organic Chemistry, 1995, vol. 60, # 13, p. 4177 - 4183
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-1-N-Boc-2-methylpiperazine(169447-70-5)1HNMR
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