ChemicalBook--->CAS DataBase List--->58421-79-7

58421-79-7

58421-79-7 Structure

58421-79-7 Structure
IdentificationBack Directory
[Name]

4-CHLORO-6-METHYLQUINAZOLINE
[CAS]

58421-79-7
[Synonyms]

AKOS BBS-00000251
IFLAB-BB F1244-0099
CHEMBRDG-BB 7188065
4-CHLORO-6-METHYLQUINAZOLINE
Quinazoline, 4-chloro-6-methyl-
[Molecular Formula]

C9H7ClN2
[MDL Number]

MFCD03665203
[MOL File]

58421-79-7.mol
[Molecular Weight]

178.62
Chemical PropertiesBack Directory
[storage temp. ]

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

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

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

P280-P305+P351+P338-P310
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
Spectrum DetailBack Directory
[Spectrum Detail]

4-CHLORO-6-METHYLQUINAZOLINE(58421-79-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-HYDROXY-6-METHYLQUINAZOLINE

19181-53-4

4-CHLORO-6-METHYLQUINAZOLINE

58421-79-7

The general procedure for the synthesis of 4-chloro-6-methylquinazoline from 6-methyl-4-hydroxyquinazoline was as follows: intermediate 10-b (2.1 g, 13.11 mmol) was dissolved in chloroform (30 ml). Oxalyl chloride (1.97 g, 23.26 mmol) and N,N-dimethylformamide (0.1 ml) were subsequently added. The reaction mixture was heated to 100°C and maintained at this temperature for 3 hours. Upon completion of the reaction, the solvent was removed by evaporation to afford intermediate 10 (1.5 g, 58% yield). Mass spectrometry analysis showed m/z = 179 ([M + H]+).

[References]

[1] Patent: WO2016/91791, 2016, A1. Location in patent: Page/Page column 20; 21
[2] Patent: WO2016/91774, 2016, A1. Location in patent: Page/Page column 23; 24
[3] Archiv der Pharmazie, 2013, vol. 346, # 1, p. 44 - 52
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