Basic information Safety Supplier Related

METHYL 6-QUINOLINEACETATE

Basic information Safety Supplier Related

METHYL 6-QUINOLINEACETATE Basic information

Product Name:
METHYL 6-QUINOLINEACETATE
Synonyms:
  • METHYL 6-QUINOLINEACETATE
  • Quinolin-6-Yl-Acetic Acid Methyl Ester
  • Methyl 6-quinolineacetate ,95%
  • Methyl 2-quinolin-6-ylacetate
  • 6-Quinolineacetic acid methyl ester
  • Methyl 2-(quinolin-6-yl)
  • methyl quinolin-6-ylacetate
CAS:
5622-36-6
MF:
C12H11NO2
MW:
201.22
Product Categories:
  • pharmacetical
  • Heterocycles
  • Acids and Derivatives
Mol File:
5622-36-6.mol
More
Less

METHYL 6-QUINOLINEACETATE Chemical Properties

Boiling point:
196-200 °C(Press: 13 Torr)
Density 
1.186±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
4.82±0.10(Predicted)
Appearance
Light yellow to brown Liquid
CAS DataBase Reference
5622-36-6
More
Less

METHYL 6-QUINOLINEACETATE Usage And Synthesis

Uses

Methyl 2-(Quinolin-6-yl)acetate is a reactuant to prepare triazolopyridazines as tyrosine kinase modulators.

Synthesis

67-56-1

5622-34-4

5622-36-6

Example 1. Preparation of methyl quinoline-6-acetate: Concentrated sulfuric acid (206 mL, 3.868 mol) was slowly added dropwise to a solution of 6-quinolineacetic acid (Compound 1001, 658.2 g, 3.516 mol, Okeanos Tech Co., Catalog No. OK-J-05024) dissolved in 6.5 L of methanol as shown in step i of Scheme 1. A slight exotherm was observed during the dropwise addition. After dropwise addition, the reaction mixture was stirred under reflux conditions for 4 hours. After completion of the reaction, it was cooled to room temperature and the volatile solvent was removed by distillation under reduced pressure. The residue was diluted with 4 L of ethyl acetate and cooled in an ice bath. Subsequently, the pH was adjusted to 4 with 2 N NaOH solution (2.1 L, 1.2 eq.) and then with saturated sodium bicarbonate solution to 8. The organic and aqueous layers were separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic phases were washed sequentially with saturated sodium bicarbonate solution, water and brine, and then dried with anhydrous MgSO4. After filtration, the solvent was evaporated under reduced pressure to give methyl quinoline-6-acetate (compound 1002, 696.8 g, 98% yield) as a clear brown oil: ESMS (M + 1), 202.14; 1H NMR (300.0 MHz, DMSO-d6) δ 8.90 (1H, dd, J = 1.7, 4.2 Hz), 8.14-8.10 (1H , m), 8.08 (1H, d, J = 8.7 Hz), 7.72 (1H, d, J = 1.4 Hz), 7.65 (1H, dd, J = 2.0, 8.7 Hz), 7.40 (1H, dd, J = 4.2, 8.3 Hz), 3.83 (2H, s), 3.73 (3H, s).

References

[1] Patent: WO2010/59668, 2010, A1. Location in patent: Page/Page column 20-21
[2] Patent: WO2016/8011, 2016, A1. Location in patent: Page/Page column 67
[3] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 117
[4] Patent: WO2008/144767, 2008, A1. Location in patent: Page/Page column 110; 115
[5] Journal of Medicinal Chemistry, 2013, vol. 56, # 17, p. 6651 - 6665

METHYL 6-QUINOLINEACETATE Preparation Products And Raw materials

Raw materials

METHYL 6-QUINOLINEACETATESupplier

ITIC MEDCHEM(SUZHOU) CO.,LTD.
Tel
0512-68323967 18015559028
Email
sales@iticmedchem.com
Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com
Shangchem Co., Ltd.
Tel
+86-21-68182121
China Langchem Inc.
Tel
0086-21-58956006
Shanghai yirong biology science and technology co., ltd
Tel
18049974220
Email
3060526242@qq.com