Basic information Description Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  6-chloro-2-methoxynicotinaldehyde

6-chloro-2-methoxynicotinaldehyde

Basic information Description Safety Supplier Related

6-chloro-2-methoxynicotinaldehyde Basic information

Product Name:
6-chloro-2-methoxynicotinaldehyde
Synonyms:
  • 6-chloro-2-methoxynicotinaldehyde
  • 6-CHLORO-2-METHOXY-PYRIDINE-3-CARBALDEHYDE
  • 6-Chloro-2-methoxy-3-pyridinecarbaldehyde
  • 6-Chloro-2-methoxypyridine-3-carboxaldehyde
  • 6-Chloro-2-methoxynicotinaldehyde 98%
  • 6-Chloro-2-methoxy-3-pyridinecarboxaldehyde
  • 3-Pyridinecarboxaldehyde, 6-chloro-2-methoxy-
CAS:
95652-81-6
MF:
C7H6ClNO2
MW:
171.58
Mol File:
95652-81-6.mol
More
Less

6-chloro-2-methoxynicotinaldehyde Chemical Properties

Melting point:
78-81°C
Boiling point:
90 °C(Press: 3 Torr)
Density 
1.317±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-1.59±0.10(Predicted)
Appearance
White to yellow Solid
InChI
InChI=1S/C7H6ClNO2/c1-11-7-5(4-10)2-3-6(8)9-7/h2-4H,1H3
InChIKey
AVBARORPQMEWPR-UHFFFAOYSA-N
SMILES
C1(OC)=NC(Cl)=CC=C1C=O
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38-43
Safety Statements 
26-36/37
WGK Germany 
3
HS Code 
2933399990
More
Less

6-chloro-2-methoxynicotinaldehyde Usage And Synthesis

Description

6-Chloro-2-methoxynicotinaldehyde is a useful research chemical.

Uses

6-chloro-2-methoxynicotinaldehyde is a heterocyclic derivative and can be used as a pharmaceutical intermediate.

Synthesis

17228-64-7

68-12-2

95652-81-6

GENERAL STEPS: 2-Chloro-6-methoxypyridine (5 g, 34.82 mmol) was dissolved in tetrahydrofuran (THF, 100 mL) under dry argon atmosphere and cooled to -78 °C. Tert-butyl lithium (tBuLi, 1.7 M, 18.5 mL, 31.34 mmol) was slowly added dropwise, keeping the temperature at -78 °C, and the reaction was stirred for 1 hour. Subsequently, N,N-dimethylformamide (DMF, 92.2 g, 31.34 mmol) was slowly added at the same temperature and stirring was continued for 2 hours. After completion of the reaction, the reaction was quenched with acetic acid and the mixture was poured into ice-cold water. The aqueous phase was alkalized with saturated sodium bicarbonate (NaHCO3) solution and subsequently extracted with ethyl acetate (EtOAc, 2 x 500 mL). The organic layers were combined, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography with the eluent being a mixed solvent of petroleum ether and ethyl acetate (10:1, v/v) to afford 6-chloro-2-methoxypyridine-3-carboxaldehyde as a white solid (3.8 g, 65% yield). The mass spectrum (ES+) showed m/z 172 [M+H]+; elemental analysis (C7H6ClNO2) was consistent with the theoretical value; 1H NMR (300 MHz, CDCl3) δ 10.17 (s, 1H), 8.07 (d, J=8.04Hz, 1H), 7.03 (d, J=8.04Hz, 1H), 3.79 (s, 3H).

References

[1] Journal of Medicinal Chemistry, 2017, vol. 60, # 13, p. 5857 - 5867
[2] Patent: US2018/65917, 2018, A1. Location in patent: Paragraph 0209
[3] Patent: EP1405859, 2004, A1. Location in patent: Page 23
[4] Organic Letters, 2014, vol. 16, # 7, p. 1980 - 1983
[5] Chemical and Pharmaceutical Bulletin, 2016, vol. 64, # 7, p. 723 - 732

6-chloro-2-methoxynicotinaldehydeSupplier

Shanghai Topbiochem Technology Co., Ltd Gold
Tel
021-58170097
Email
info@topbiochem.com
Shanghai Wishpharma Co.,Ltd. Gold
Tel
021-56789108 18694901298
Email
95413064@qq.com
PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Email
sales@pharmablock.com
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Email
sales@accelachem.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com