ChemicalBook--->CAS DataBase List--->120737-78-2

120737-78-2

120737-78-2 Structure

120737-78-2 Structure
IdentificationMore
[Name]

1-Boc-2-Methylpiperazine
[CAS]

120737-78-2
[Synonyms]

(+/-)-1-N-BOC-2-METHYL PIPERAZINE
1-N-BOC-2-METHYLPIPERAZINE
2-METHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
N-1-BOC-2-METHYLPIPERAZINE
N-4-BOC-3-METHYL-PIPERAZINE
TERT-BUTYL-2-METHYL-1-PIPERAZINECARBOXYLATE
TERT-BUTYL 2-METHYLPIPERAZINE-1-CARBOXYLATE
4-N-Boc-3-methylpiperazine
1-Boc-2-Methylpiperazine
1-N-Boc-2-methyl-piperizine
N-4-BOC-3-METHYLPIPERIZINE
[Molecular Formula]

C10H20N2O2
[MDL Number]

MFCD02179168
[Molecular Weight]

200.28
[MOL File]

120737-78-2.mol
Chemical PropertiesBack Directory
[Boiling point ]

268.7±15.0 °C(Predicted)
[density ]

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

under inert gas (nitrogen or Argon) at 2–8 °C
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oil
[pka]

8.49±0.40(Predicted)
[color ]

Colourless
[CAS DataBase Reference]

120737-78-2(CAS DataBase Reference)
Safety DataBack Directory
[RIDADR ]

2735
[HazardClass ]

IRRITANT
[PackingGroup ]

Ⅲ
[HS Code ]

2933599590
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Tetrahydrofuran-->Dichloromethane-->Lithium Aluminum Hydride-->Di-tert-butyl dicarbonate-->Trifluoroacetic acid-->Triphenylphosphine-->1,1'-Carbonyldiimidazole-->DL-Alanine-->Diethyl azodicarboxylate-->N-Benzylethanolamine
Hazard InformationBack Directory
[Uses]

tert-Butyl 2-methylpiperazine-1-carboxylate is a useful reagent used in the synthesis of anthrafuran carboxamides with antitumor properties.
[Synthesis]

1-BENZYL-4-BOC-PIPERAZINE

120737-77-1

1-Boc-2-Methylpiperazine

120737-78-2

General procedure for the synthesis of tert-butyl 2-methylpiperazine-1-carboxylate from the compound (CAS: 120737-77-1): a mixture of tert-butyl (RS)-4-benzyl-2-methylpiperazine-1-carboxylate (3.41 g, 11.7 mmol), ethanol (125 mL), and Pearlman's catalyst (0.854 g, 6.08 mmol) was was hydrogenated overnight at 36 psi pressure at ambient temperature. Upon completion of the reaction, the mixture was filtered and the solids were washed sequentially with ethanol, dichloromethane (DCM) and methanol (MeOH). The filtrate and washings were combined, concentrated in vacuum, redissolved in dichloromethane, filtered again and concentrated in vacuum to give tert-butyl 2-methylpiperazine-1-carboxylate as a beige oil (2.0 g, 86% yield). The nuclear magnetic resonance (NMR) spectrum of the product was in agreement with the data reported in the literature (J. Org. Chem. 1995, 60, 4183).

[References]

[1] Patent: WO2007/135427, 2007, A1. Location in patent: Page/Page column 31
[2] Patent: US4880808, 1989, A
Spectrum DetailBack Directory
[Spectrum Detail]

1-Boc-2-Methylpiperazine(120737-78-2)1HNMR
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