ChemicalBook--->CAS DataBase List--->635712-99-1

635712-99-1

635712-99-1 Structure

635712-99-1 Structure
IdentificationBack Directory
[Name]

6-(BENZYLOXY)NICOTINALDEHYDE
[CAS]

635712-99-1
[Synonyms]

6-(BENZYLOXY)NICOTINALDEHYDE
6-Benzyloxypyridine-3-carboxaldehyde
6-Phenylmethoxypyridine-3-carbaldehyde
3-Pyridinecarboxaldehyde, 6-(phenylmethoxy)-
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C13H11NO2
[MDL Number]

MFCD10697656
[MOL File]

635712-99-1.mol
[Molecular Weight]

213.23
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Hazard InformationBack Directory
[Synthesis]

2-BENZYLOXY-5-BROMOPYRIDINE

83664-33-9

N,N-Dimethylformamide

68-12-2

6-(BENZYLOXY)NICOTINALDEHYDE

635712-99-1

General procedure for the synthesis of 6-(benzyloxy)nicotinaldehyde from 2-benzyloxy-5-bromopyridine and N,N-dimethylformamide: n-butyllithium (2.5 M hexane solution, 2.61 mL, 1.05 eq.) was slowly added to a tetrahydrofuran solution (25 mL, -78 °C) of 2-benzyloxy-5-bromopyridine (1.64 g, 6.2 mmol). After 1 hour of reaction at -78 °C, N,N-dimethylformamide (0.97 mL, 2 eq.) was added and stirring was continued at -78 °C for 30 minutes. The reaction mixture was rapidly poured into a stirring 5% aqueous sodium bicarbonate solution (50 mL) and extracted with ether (3 x 50 mL). The organic phases were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated to give a crude product of 1.16 g (quantitative yield), which could be used in the next reaction without further purification. Mass spectrometry analysis showed a molecular ion peak of 186.34 ([MH]+) for the target compound.

[References]

[1] Patent: WO2003/104236, 2003, A1. Location in patent: Page 169
[2] Polyhedron, 2013, vol. 52, p. 755 - 760
[3] Journal of Medicinal Chemistry, 2014, vol. 57, # 6, p. 2536 - 2548
[4] Patent: WO2004/92145, 2004, A1. Location in patent: Page 149
[5] Patent: US2009/82403, 2009, A1. Location in patent: Page/Page column 66
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