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68947-43-3

68947-43-3 Structure

68947-43-3 Structure
IdentificationBack Directory
[Name]

1-METHYL-PIPERIDINE-4-CARBOXYLIC ACID
[CAS]

68947-43-3
[Synonyms]

N-Methylisonipecotic acid
4-Carboxy-1-methylpiperidine
N-METHYLPIPERIDINE-4-CARBOXYLIC ACID
1-METHYL-PIPERIDIN-4-CARBOXYLIC ACID
1-METHYL-PIPERIDINE-4-CARBOXYLIC ACID
N-METHYL-4-PIPERIDINE CARBOXYLIC ACID
1-methyl-Ppiperidine-4-carboxylic'acid
1-methylpiperidine-4-carboxylic acid(SALTDATA: HCl)
[Molecular Formula]

C7H13NO2
[MDL Number]

MFCD06659473
[MOL File]

68947-43-3.mol
[Molecular Weight]

143.18
Chemical PropertiesBack Directory
[Boiling point ]

246.1±33.0 °C(Predicted)
[density ]

1.103
[refractive index ]

1.488
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

3.16±0.20(Predicted)
[color ]

Pale yellow
[InChI]

InChI=1S/C7H13NO2/c1-8-4-2-6(3-5-8)7(9)10/h6H,2-5H2,1H3,(H,9,10)
[InChIKey]

HCKNAJXCHMACDN-UHFFFAOYSA-N
[SMILES]

N1(C)CCC(C(O)=O)CC1
Questions And AnswerBack Directory
[Uses]

1-Methylpiperidine-4-carboxylic acid is a heterocyclic organic compound and can be used as a pharmaceutical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P271-P260-P280
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

29333990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl 1-methyl-4-piperidinecarboxylate-->Water-->Hydrogen
[Preparation Products]

N-Methoxy-N,1-diMethylpiperidine-4-carboxaMide-->4-Piperidinecarbonyl chloride, 1-methyl- (9CI)
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Synthesis]

Isonipecotic acid

498-94-2

Formaldehyde

50-00-0

1-METHYL-PIPERIDINE-4-CARBOXYLIC ACID

68947-43-3

Using 4-piperidinecarboxylic acid (1 kg, 7.74 mol) and formaldehyde (37% aqueous solution, 720 g, 8.87 mol, 1.15 eq.) as feedstock, a wet Pd/C catalyst (10%; 55% paste, 100 g) was added to 10 L of water and the mixture was transferred to a stainless steel hydrogenation reactor. The reactor was pressurized with hydrogen (3 bar) and the reaction mixture was reacted overnight at 16-25 °C with a stirring speed of 200-2500 rpm. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was washed with 500 mL of water and subsequently concentrated under vacuum. The residue was azeotropically distilled by ethanol (2 x 1 L) to remove residual water. Finally, the resulting solid was dried under vacuum at 50 °C overnight to afford 1-methylpiperidine-4-carboxylic acid as an off-white solid (1087 g, 98.1% yield).

[References]

[1] Patent: WO2003/84949, 2003, A1. Location in patent: Page/Page column 45; 46
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 22, p. 10118 - 10129
[3] Patent: US6777428, 2004, B1. Location in patent: Page column 24
[4] Journal of Medicinal Chemistry, 1993, vol. 36, # 4, p. 449 - 459
[5] Patent: WO2008/62182, 2008, A1. Location in patent: Page/Page column 161-162
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHYL-PIPERIDINE-4-CARBOXYLIC ACID(68947-43-3)1HNMR
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