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111247-60-0

111247-60-0 Structure

111247-60-0 Structure
IdentificationBack Directory
[Name]

1-PYRIMIDIN-2-YL-PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER
[CAS]

111247-60-0
[Synonyms]

BUTTPARK 90\06-42
ETHYL1-PYRIMIDIN-2-YLPIPERIDINE-4-CARBOXYLATE
Ethyl 1-pyrimidin-2-ylpiperidine-4-carboxylate 95+%
1-Pyrimidin-2-yl-piperidine-4-carboxylicacidethylester95%
1-PYRIMIDIN-2-YL-PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER
1-(2-pyrimidinyl)-4-piperidinecarboxylic acid ethyl ester
4-Piperidinecarboxylic acid, 1-(2-pyriMidinyl)-, ethyl ester
1-PYRIMIDIN-2-YL-PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER 95%
1-PYRIMIDIN-2-YL-PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER ISO 9001:2015 REACH
[Molecular Formula]

C12H17N3O2
[MDL Number]

MFCD01456221
[MOL File]

111247-60-0.mol
[Molecular Weight]

235.28
Chemical PropertiesBack Directory
[Boiling point ]

373.4±52.0 °C(Predicted)
[density ]

1.163±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

5.04±0.33(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2933599590
Hazard InformationBack Directory
[Synthesis]

2-Chloropyrimidine

1722-12-9

Ethyl 4-piperidinecarboxylate

1126-09-6

1-PYRIMIDIN-2-YL-PIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER

111247-60-0

2-Chloropyrimidine (2.28 g, 20 mmol) and ethyl 4-piperidinecarboxylate (4.72 g, 30 mmol) were mixed in toluene (10 mL) and heated to reflux for 18 hours. After completion of the reaction, the mixture was cooled to room temperature, diluted with ethyl acetate and washed with saturated aqueous sodium bicarbonate. The organic layer was separated, dried and the solvent was removed under vacuum. The residue was purified by rapid chromatography on silica gel (eluent: ethyl acetate/petroleum ether, 40/60, v/v) to afford ethyl 1-(2-pyrimidinyl)piperidine-4-carboxylate as a colorless oil in a yield of 4.00 g in 81%. Mass spectrum (ESI+): [M + H]+ = 236.0.

[References]

[1] Farmaco, 1993, vol. 48, # 10, p. 1439 - 1445
[2] Patent: WO2010/97576, 2010, A1. Location in patent: Page/Page column 39
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 21, p. 8696 - 8711
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