ChemicalBook--->CAS DataBase List--->206258-97-1

206258-97-1

206258-97-1 Structure

206258-97-1 Structure
IdentificationBack Directory
[Name]

8-Bromo-4-chloroquinoline-3-carboxylic acid ethyl ester
[CAS]

206258-97-1
[Synonyms]

CAS:206258-97-1
Ethyl 4-chloro-8-broMoquinoline-3-carboxylate
Ethyl8-bromo-4-chloroquinoline-3-carboxylate,97%
ethyl 8-bromo-4-chloroquinoline-3-carboxylate - [E5351]
8-Bromo-4-chloroquinoline-3-carboxylic acid ethyl ester
8-Bromo-4-chloro-3-quinolinecarboxylic acid ethyl ester
3-Quinolinecarboxylic acid, 8-bromo-4-chloro-, ethyl ester
[Molecular Formula]

C12H9BrClNO2
[MDL Number]

MFCD00173385
[MOL File]

206258-97-1.mol
[Molecular Weight]

314.562
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C12H9BrClNO2/c1-2-17-12(16)8-6-15-11-7(10(8)14)4-3-5-9(11)13/h3-6H,2H2,1H3
[InChIKey]

MLHAFVCMBUQWKC-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC=CC=2Br)C(Cl)=C(C(OCC)=O)C=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[WGK Germany ]

3
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

8-Bromo-4-chloroquinoline-3-carboxylic acid ethyl ester(206258-97-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL 8-BROMO-4-HYDROXYQUINOLINE-3-CARBOXYLATE

35975-57-6

8-Bromo-4-chloroquinoline-3-carboxylic acid ethyl ester

206258-97-1

General procedure for the synthesis of ethyl 4-chloro-8-bromoquinoline-3-carboxylate from ethyl 4-hydroxy-8-bromoquinoline-3-carboxylate: ethyl 8-bromo-4-hydroxyquinoline-3-carboxylate (2.0 g, 6.75 mmol) was dissolved in phosphorus triclosan (10 mL) and heated to reflux for 3 hr at 80 °C. Upon completion of the reaction, volatiles were removed by distillation under reduced pressure and the residue was quenched with ice water. The precipitated solid was collected by filtration and dried to give 1.8 g of the target product ethyl 4-chloro-8-bromoquinoline-3-carboxylate. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6) and mass spectrometry: 1H NMR δ 9.26 (s, 1H), 8.44-8.37 (m, 2H), 7.79-7.64 (t, J = 7.8 Hz, 1H), 4.48-4.43 (q, J = 7.2, 14.1 Hz, 2H), 1.41-1.36 (t. J = 6.9 Hz, 3H); MS (m/z): 314.01 (M + H)+.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 8, p. 1487 - 1490
[2] Patent: US2013/210844, 2013, A1. Location in patent: Paragraph 0338; 0339
[3] Patent: CN108623590, 2018, A. Location in patent: Paragraph 0149
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