ChemicalBook--->CAS DataBase List--->651057-01-1

651057-01-1

651057-01-1 Structure

651057-01-1 Structure
IdentificationBack Directory
[Name]

1-(METHYLSULFONYL)PIPERIDIN-4-AMINE HYDROCHLORIDE
[CAS]

651057-01-1
[Synonyms]

1-(Methylsulfonyl)-4-piperidinaMine HCl
1-(Methylsulfonyl)piperidin-4-amine, HCl
1-(METHYLSULFONYL)PIPERIDIN-4-AMINE HCl SALT
1-methylsulfonyl-4-piperidinamine hydrochloride
1-Methanesulfonylpiperidin-4-aMine hydrochloride
1-(METHYLSULFONYL)PIPERIDIN-4-AMINE HYDROCHLORIDE
4-Amino-1-(methylsulfonyl)piperidine Hydrochloride
1-METHANESULFONYL-PIPERIDIN-4-YLAMINE HYDROCHLORIDE
4-AMino-1-(Methanesulfonyl)piperidine hydrochloride
[Molecular Formula]

C6H15ClN2O2S
[MDL Number]

MFCD08690153
[MOL File]

651057-01-1.mol
[Molecular Weight]

214.714
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C6H14N2O2S.ClH/c1-11(9,10)8-4-2-6(7)3-5-8;/h6H,2-5,7H2,1H3;1H
[InChIKey]

BASBDQBWDDKEDK-UHFFFAOYSA-N
[SMILES]

N1(S(C)(=O)=O)CCC(N)CC1.Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

24/25
[HazardClass ]

IRRITANT
[HS Code ]

29339900
Spectrum DetailBack Directory
[Spectrum Detail]

1-(METHYLSULFONYL)PIPERIDIN-4-AMINE HYDROCHLORIDE(651057-01-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

tert-Butyl (1-(Methylsulfonyl)piperidin-4-yl)carbaMate

287953-38-2

1-(METHYLSULFONYL)PIPERIDIN-4-AMINE HYDROCHLORIDE

651057-01-1

The general procedure for the synthesis of 1-methylsulfonyl-4-aminopiperidine hydrochloride from 1-MS-4-Boc-aminopiperidine was as follows: 4-(N-Boc-amino)-1-methanesulfonylpiperidine (3.1 g, 11.15 mmol) was dissolved in 4 M HCl/dioxane solution (40 ml) and the reaction was stirred for 24 h at room temperature. After completion of the reaction, the reaction mixture was concentrated in vacuum. The resulting residue was azeotropically dried by mixing with toluene:methanol (1:1, v/v) to give the final 1-methylsulfonyl-piperidin-4-ylamine hydrochloride as a white solid (2.4 g, 100% yield).

[References]

[1] Patent: WO2006/77414, 2006, A1. Location in patent: Page/Page column 164
[2] Patent: EP2261213, 2010, A1. Location in patent: Page/Page column 44-45
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