212143-48-1

Basic information

• Product Name: 2-(Methylsulfinyl)quinazolin-4(3H)-one
• Synonyms: 2-(Methylsulfinyl)quinazolin-4(3H)-one
• CAS NO: 212143-48-1
• Molecular Formula: C9H8N2O2S
• Molecular Weight: 208.23702
• Mol File: 212143-48-1.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(Methylsulfinyl)quinazolin-4(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(Methylsulfinyl)quinazolin-4(3H)-one(212143-48-1)
• EPA Substance Registry System: 2-(Methylsulfinyl)quinazolin-4(3H)-one(212143-48-1)

Safety Data

• Hazardous Substances Data: 212143-48-1(Hazardous Substances Data)

Upstream product

• 13906-09-7 2-mercapto-3H-quinazolin-4-one 
• 28144-70-9 anthranilic acid amide 
• 54855-81-1 2-methylthioquinazolin-4(3H)-one 

Relevant articles and documents

Studies on quinazolines and 1,2,4-benzothiadiazine 1,1-dioxides. 8. Synthesis and pharmacological evaluation of tricyclic fused quinazolines and 1,2,4-benzothiadiazine 1,1-dioxides as potential α1-adrenoceptor antagonists

A series of 2-substituted methyl 2,3-dihydroimidazo[1,2-c]quinazolin- 5(6H)-ones (4), 3-substituted methyl 2,3-dihydroimidazo[1,2-c]quinazolin- 5(6H)-ones (5), 3-substituted methyl 2,3-dihydro-5H-thiazolo[2,3- b]quinazolin-5-ones (15a,b), 3-substituted methyl 2,3-dihydroimidazo[2,1- b]quinazolin-5(1H)-ones (16a,b), 3-substituted methyl 2,3-dihydro-1H- imidazo[1,2-b][1,2,4]benzothiadiazine 5,5-dioxides (33a,b), 2-substituted methyl imidazo[1,2-c]quinazolin-5(6H)-ones (42-45a,b), 3-substituted methyl imidazo[1,2-c]quinazolin-5(6H)-ones (50-53a,b), 3-substituted methyl 5H- thiazolo[2,3-b]quinazolin-5-ones (55-56a,b), and 3-substituted methyl 5- (methylthio)-2,3-dihydroimidazo[1,2-c]quinazoline (57) were synthesized as compound 1 conformational rigid congeners for pharmacological evaluation as potential α1-adrenoceptor antagonists. Compounds 4, 5, 33a,b, 44a,b, 45a,b, 52a,b, 53a,b, and 57 were found to possess high affinity for the α1- adrenoceptor. Compounds 5 and 57 were the most highly selective and potent α1 antagonists with K(i) = 0.21 ± 0.02 and 0.90 ± 0.08 nM, respectively. The S-enantiomers of these two compounds (K(i) = 0.13 ± 0.01 nM for (S)-(- )-5; K(i) = 1.0 ± 0.2 nM for (S)-(+)-57) were 144-200-fold more potent than the R-enantiomers (K(i) = 26 ± 8 nM for (R)-(+)-5; K(i) = 144 ± 23 nM for (R)-(-)-57). Compound 4 showed 8-fold higher affinity to α1A-AR better than α1B-AR. These compounds possessed weak to no activity against the 5-HT1A receptor.