ChemicalBook--->CAS DataBase List--->39267-04-4

39267-04-4

39267-04-4 Structure

39267-04-4 Structure
IdentificationBack Directory
[Name]

2,3-Dichloro-6-methoxyquinoxaline
[CAS]

39267-04-4
[Synonyms]

EOS-61016
Grazoprevir Intermediate 1
Quinoxaline, 2,3-dichloro-6-Methoxy-
2,3-Dichloro-6-methoxyquinoxaline 98%
2,3-Dichloro-6-methoxy-1,4-benzodiazine
[Molecular Formula]

C9H6Cl2N2O
[MDL Number]

MFCD00461063
[MOL File]

39267-04-4.mol
[Molecular Weight]

229.06
Chemical PropertiesBack Directory
[density ]

1.450
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

White to pink Solid
[InChI]

InChI=1S/C9H6Cl2N2O/c1-14-5-2-3-6-7(4-5)13-9(11)8(10)12-6/h2-4H,1H3
[InChIKey]

NFJQDGNCJJPQNV-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC(OC)=CC=2)N=C(Cl)C=1Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

2,3-Dichloro-6-methoxyquinoxaline is used for preparation of antibacterial and antifungal activity of (tetrazolo[1,5-a]quinoxalinyl)dihydrophthalazine-diones as reactant or reagent.
[Synthesis]

2,3-DIHYDROXY-6-METHOXYQUINOXALINE

31910-18-6

2,3-Dichloro-6-methoxyquinoxaline

39267-04-4

General procedure for the synthesis of 2,3-dichloro-6-methoxyquinoxaline from 6-methoxyquinoxaline-2,3-diol: 6-methoxy-1,4-dihydro-quinoxaline-2,3-dione (15.5 g, 1 mmol) was dissolved in 75 mL of phosphorochloride, and the reaction mixture was heated and refluxed for 24 hours. Upon completion of the reaction, a 1:1 mixture of water and methanol was slowly added at 0 to 5 °C to quench the reaction. Subsequently, the resulting precipitate was collected by filtration and dried under reduced pressure to give 17.2 g of 2,3-dichloro-6-methoxyquinoxaline in 93.1% yield.

[References]

[1] Patent: KR2018/106597, 2018, A. Location in patent: Paragraph 0451-0454
[2] Journal of Medicinal Chemistry, 2011, vol. 54, # 13, p. 4508 - 4522
[3] Journal of Medicinal Chemistry, 1990, vol. 33, # 8, p. 2240 - 2254
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