Anodyne

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Diproqualone
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Physical properties
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234.25 g/mol [1]
-0.4 [1]
Structural Identifiers
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C12H14N2O3 [1]
3-(2,3-dihydroxypropyl)-2-methylquinazolin-4-one [1]
CC1=NC2=CC=CC=C2C(=O)N1CC(CO)O [1]
InChI=1S/C12H14N2O3/c1-8-13-11-5-3-2-4-10(11)12(17)14(8)6-9(16)7-15/h2-5,9,15-16H,6-7H2,1H3 [1]
InChIKeyNTGLQWGMESPVBV-UHFFFAOYSA-N [1]

Diproqualone

Diproqualone (also known as Diprocualona, Diproqualone, (+)-, L2Y2CV3EW7, 3-(2,3-Dihydroxypropyl)-2-methyl-4(3H)-quinazolinone, 3-(2,3-Dihydroxypropyl)-2-methyl-3,4-dihydroquinazolin-4-one, 46800-89-9, Diproqualonum, 4(3H)-Quinazolinone, 3-(2,3-dihydroxypropyl)-2-methyl-, (+)-, Diproqualon or 3-(2,3-dihydroxypropyl)-2-methylquinazolin-4(3h)-one) is a sedative substance of the quinazolinone class.

Chemistry

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Diproqualone is a racemic mixture of the optical stereoisomers

Stereoisomers
(+)-DiproqualoneGenerated by the Chemistry Development Kit (http://github.com/cdk)
(-)-DiproqualoneGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • Substituted quinazolinones
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 64112, Diproqualone. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/64112

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Diproqualone. UNII: QY7HLH8V4L. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/QY7HLH8V4L