Bhargava, P. N.; Prakash, Shree published the artcile< Synthesis of S-substituted-2-mercapto-3-aryl (or aralkyl)-4 (3H) quinazolinones: their CNS and antimicrobial activity>, Related Products of 5326-82-9, the main research area is quinazolinylthioacetamide; thioacetamide quinazolinyl; acetamide quinazolinylthio; central stimulant quinazolinylthioacetamide; bactericide quinazolinylthioacetamide; fungicide quinazolinylthioacetamide; quinazolinethiol chloroacetamide.
Quinazolinylthioacetamides I (R = Ph, 2-MeC6H4, 4-ClC6H4, 4-MeOC6H4, 4-EtOC6H4, R1 = CH2CHMe2, CH2Ph; R = 4-MeC6H4, R1 = CH2CHMe2; R = 3-MeC6H4, PhCH2, R1 = CH2Ph) were obtained by treating quinazolinethiols with ClCH2CONR12. I increased spontaneous motor activity in mice at 600 mg/kg but had no bactericidal or fungicidal activity.
Indian Journal of Pharmacy published new progress about Central nervous system stimulants. 5326-82-9 belongs to class amides-buliding-blocks, and the molecular formula is C10H20ClNO, Related Products of 5326-82-9.
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics