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Methyl 6-quinolineacetate

CAS No.
5622-36-6
Chemical Name:
Methyl 6-quinolineacetate
Synonyms
Methyl 2-(quinolin-6-yl);Methyl 6-quinolineacetate;methyl quinolin-6-ylacetate;Methyl 2-quinolin-6-ylacetate;Methyl 6-quinolineacetate ,95%;6-Quinolineacetic acid methyl ester;Quinolin-6-Yl-Acetic Acid Methyl Ester
CBNumber:
CB0121284
Molecular Formula:
C12H11NO2
Molecular Weight:
201.22
MDL Number:
MFCD04038669
MOL File:
5622-36-6.mol
Last updated:2026-09-12 18:43:53

Methyl 6-quinolineacetate 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

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315
Precautionary statements  P280

Methyl 6-quinolineacetate price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Synthonix M38116 Methyl 2-(quinolin-6-yl)acetate 95+% 5622-36-6 100mg $18 2026-05-06 Buy
Synthonix M38116 Methyl 2-(quinolin-6-yl)acetate 95+% 5622-36-6 250mg $24 2026-05-06 Buy
Synthonix M38116 Methyl 2-(quinolin-6-yl)acetate 95+% 5622-36-6 1g $40 2026-05-06 Buy
Synthonix M38116 Methyl 2-(quinolin-6-yl)acetate 95+% 5622-36-6 5g $110 2026-05-06 Buy
Synthonix M38116 Methyl 2-(quinolin-6-yl)acetate 95+% 5622-36-6 10g $190 2026-05-06 Buy
Product number Packaging Price Buy
M38116 100mg $18 Buy
M38116 250mg $24 Buy
M38116 1g $40 Buy
M38116 5g $110 Buy
M38116 10g $190 Buy

Methyl 6-quinolineacetate Chemical Properties,Uses,Production

Uses

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

Synthesis

Methanol

67-56-1

6-QUINOLINEACETIC ACID

5622-34-4

METHYL 6-QUINOLINEACETATE

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

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Methyl 6-quinolineacetate Spectrum

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 Methyl 6-quinolineacetate 5622-36-6 pharmacetical Heterocycles Acids and Derivatives