ChemicalBook--->CAS DataBase List--->180609-56-7

180609-56-7

180609-56-7 Structure

180609-56-7 Structure
IdentificationBack Directory
[Name]

Benzyl 2-methylpiperidine-1,2-dicarboxylate
[CAS]

180609-56-7
[Synonyms]

Methyl 1-Cbz-piperidine-2-carboxylate
Benzyl 2-methylpiperidine-1,2-dicarboxylate
1-benzyl 2-methyl piperidine-1,2-dicarboxylate
1,2-Piperidinedicarboxylic acid 2-methyl-1-(phenylmethyl)ester
[Molecular Formula]

C15H19NO4
[MOL File]

180609-56-7.mol
[Molecular Weight]

277.32
Chemical PropertiesBack Directory
[Boiling point ]

390.4±42.0 °C(Predicted)
[density ]

1.187
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

-3.33±0.40(Predicted)
[Appearance]

Light yellow to yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

Benzyl 2-methylpiperidine-1,2-dicarboxylate(180609-56-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-CBZ-2-PIPERIDINECARBOXYLIC ACID

28697-07-6

Iodomethane

74-88-4

Benzyl 2-methylpiperidine-1,2-dicarboxylate

180609-56-7

Example 36; 2-(2-methylpiperidin-2-yl)-1H-benzimidazole-4-carboxamide; Example 36A; 1-Benzyl-2-methylpiperidine-1,2-dicarboxylate. 1-[(Benzyloxy)carbonyl]piperidine-2-carboxylic acid (5 g) and iodomethane (2.5 mL) were dissolved in DMF (40 mL), potassium bicarbonate (3.8 g) was added, and the reaction mixture was stirred for 18 hours at room temperature. Upon completion of the reaction, the reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The organic phase was separated, concentrated and the residue was purified by fast chromatography (silica gel, ethyl acetate/hexane as eluent) to give Example 36A (4.88 g, yield: 93%). The mass spectrum (DCI/NH3) showed m/z 278 (M + H)+.

[References]

[1] Patent: US2006/229289, 2006, A1. Location in patent: Page/Page column 20-21
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