(S)-3-N-Boc-3-(methylamino)piperidine Chemical Properties

Boiling point:

288℃

Density 

1.01

Flash point:

128℃

storage temp. 

2-8°C(protect from light)

pka

9.74±0.10(Predicted)

Appearance

Colorless to light yellow Viscous liquid

Safety Information

Risk Statements 

36/37/38

Safety Statements 

26-37

HS Code 

29333990

(S)-3-N-Boc-3-(methylamino)piperidine Usage And Synthesis

Chemical Properties

Light yellow viscid liquid

Uses

(S)-tert-Butyl methyl(piperidin-3-yl)carbamate is a useful reactant for the synthesis substituted azoles, thiophenes and furans that act as sterol regulatory element-?binding proteins (SREBPs) inhibitors.

Synthesis

The product of Example 42A (1.78 g, 6.0 mmol) was dissolved in THF (30 mL) at 0 °C and NaH (0.360 g, 60% dispersion, 9.0 mmol) was added. After stirring for 20 min, iodomethane (1.12 mL, 18 mmol) was added dropwise to the mixture, followed by slow warming of the reaction system to room temperature. After continued stirring for 4 hours, methanol (5 mL) was slowly added to quench the reaction, followed by concentration of the reaction mixture under reduced pressure. The concentrated residue was dissolved in fresh methanol (50 mL) and 20% aqueous K2CO3 (5 mL) was added. After stirring at room temperature for 16 hours, the mixture was concentrated under reduced pressure. The residue was extracted by partitioning with dichloromethane (50 mL) and saturated saline (20 mL). The organic phase was separated, dried with anhydrous MgSO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane/methanol/ammonia, 95:5:0.5, v/v/v) to afford the title compound (S)-3-N-BOC-3-(methylamino)piperidine as a hygroscopic yellow solid (1.14 g, 93% yield). Mass spectrum (chemical ionization/NH3) m/z 215 ([M+H]+).

References

[1] Patent: EP1428824, 2004, A1. Location in patent: Page 45

(S)-3-N-Boc-3-(methylamino)piperidine(309962-63-8)Related Product Information

• (S)-1-Boc-piperidine-2-carboxylic acid
• 3-N-BOC-3-(METHYLAMINO)PIPERIDINE
• (S)-3-N-Boc-3-(methylamino)piperidine
• (S)-3-N-Boc-aminopiperidine
• (1S,4S)-2-BOC-2,5-DIAZABICYCLO[2.2.2]OCTANE HYDROCHLORIDE
• (1S,4S)-2-BOC-2,5-DIAZABICYCLO(2.2.2)OCTANE
• METHYL-3-PIPERIDINYL-CARBAMIC ACID ETHYL ESTER