ChemicalBook--->CAS DataBase List--->67074-63-9

67074-63-9

67074-63-9 Structure

67074-63-9 Structure
IdentificationBack Directory
[Name]

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE
[CAS]

67074-63-9
[Synonyms]

4-Methyl-3,4-dihydroquinoxalin-2(1H)
4-methyl-1,3-dihydroquinoxalin-2-one
4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE
3,4-dihydro-4-methyl-2(1H)-Quinoxalinone
2(1H)-Quinoxalinone, 3,4-dihydro-4-methyl-
[Molecular Formula]

C9H10N2O
[MDL Number]

MFCD13152341
[MOL File]

67074-63-9.mol
[Molecular Weight]

162.19
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE(67074-63-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Formaldehyde

50-00-0

3,4-Dihydro-1H-quinoxalin-2-one

59564-59-9

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE

67074-63-9

The general procedure for the synthesis of 4-methyl-3,4-dihydroquinoxalin-2(1H)-one from formaldehyde and 3,4-dihydroquinoxalin-2(1H)-one was as follows: sodium cyanoborohydride (425 mg, 6.76 mmol) was sequentially added to a methanol (3 mL) solution of 3,4-dihydroquinoxalin-2(1H)-one (500 mg, 3.378 mmol), paraformaldehyde (102 mg) and acetic acid (30 μL). The reaction mixture was stirred at room temperature for 4 hours. Subsequently, another portion of sodium cyanoborohydride (212 mg, 3.37 mmol), paraformaldehyde (51 mg) and concentrated hydrochloric acid (10 μL) was added to the reaction mixture. The reaction mixture was stirred at 50 °C for 5 h and then cooled to room temperature. The pH was adjusted to 8 with base and the solvent was evaporated under reduced pressure. The target product was extracted with ethyl acetate and washed with brine and dried over anhydrous sodium sulfate. After evaporation of the solvent under reduced pressure, 4-methyl-3,4-dihydroquinoxalin-2(1H)-one (537 mg, 98% yield) was obtained as a beige powder.LC-MS ESI m/z 163 [M + H]+.

[References]

[1] Patent: US2005/261244, 2005, A1. Location in patent: Page/Page column 53
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 22, p. 9275 - 9295
[3] Patent: CN106317027, 2017, A. Location in patent: Paragraph 0196; 0197; 0198
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