BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE

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CAS:159275-17-9
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CAS:159275-17-9
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BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE manufacturers

BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE Basic information
Product Name:BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE
Synonyms:N-(BENZYLOXYCARBONYL)-4-(BROMOMETHYL)PIPERIDINE;BENZYL 4-(BROMOMETHYL)PIPERIDINE-1-CARBOXYLATE;BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE;BUTTPARK 95\50-67;Benzyl 4-(bromoethyl)tetrahydro-1(2H)-pyridinecarboxylate;4-(Bromomethyl)piperidine, N-CBZ protected;N-(Benzyloxycarbonyl)-4-(bromomethyl)piperidine, 98 %;1-CBZ-4-(BROMOMETHYL)PIPERIDINE
CAS:159275-17-9
MF:C14H18BrNO2
MW:312.2
EINECS:
Product Categories:Methyl Halides;Pyrans, Piperidines & Piperazines;Methyl Halides;Pyrans, Piperidines &Piperazines;Piperidine;API intermediates;Halides;Heterocycles
Mol File:159275-17-9.mol
BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE Structure
BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE Chemical Properties
Melting point 68 °C
Boiling point 403.4±28.0 °C(Predicted)
density 1.356±0.06 g/cm3(Predicted)
storage temp. 2-8°C, stored under nitrogen
pka-1.96±0.40(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C14H18BrNO2/c15-10-12-6-8-16(9-7-12)14(17)18-11-13-4-2-1-3-5-13/h1-5,12H,6-11H2
InChIKeyXJHKDSZGAWXUTB-UHFFFAOYSA-N
SMILESN1(C(OCC2=CC=CC=C2)=O)CCC(CBr)CC1
CAS DataBase Reference159275-17-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38-34
Safety Statements 26-36/37/39-45
Hazard Note Irritant
HS Code 2933399990
MSDS Information
BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE Usage And Synthesis
Synthesis
1-Cbz-4-hydroxymethylpiperidine

122860-33-7

BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE

159275-17-9

Under nitrogen atmosphere, benzyl 4-(hydroxymethyl)piperidine-1-carboxylate (10 g, 40.11 mmol) was added to a 500 mL three-necked round-bottomed flask, dissolved in dichloromethane (100 mL), and the mixture was cooled to 0 °C. Subsequently, a solution of triphenylphosphine (13.7 g, 52.14 mmol) in dichloromethane (50 mL) was slowly added to the reaction mixture and kept stirring at 0°C for 20 minutes. Next, a dichloromethane (50 mL) solution of carbon tetrabromide (16 g, 48.13 mmol) was added and the reaction mixture was brought to room temperature and stirred for 3 hours. Upon completion of the reaction, the reaction mixture was diluted with dichloromethane and washed with deionized water. The organic layer was separated, dried with anhydrous sodium sulfate and concentrated under reduced pressure. Finally, purification by column chromatography afforded benzyl 4-(bromomethyl)piperidine-1-carboxylate (10 g).

References[1] Journal of Medicinal Chemistry, 2005, vol. 48, # 10, p. 3586 - 3604
[2] Journal of Medicinal Chemistry, 2003, vol. 46, # 13, p. 2606 - 2620
[3] Patent: WO2015/195950, A1. Location in patent: Page/Page column 82
[3] Patent: , 2015, . Location in patent: Page/Page column 82
BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Methanol-->Tetrahydrofuran-->Triphenylphosphine-->Phosphorus tribromide-->Sulfuryl chloride-->Benzyl chloroformate-->Isonipecotic acid-->Lithium borohydride-->4-Piperidinemethanol-->Carbon tetrabromide
Tag:BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE(159275-17-9) Related Product Information
Benzyl formate BENZYL 4-(BROMOMETHYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE BENZYL (4-BROMOBUTYL)CARBAMATE