35700-51-7

Upstream product

• 108367-90-4 (4-dimethylamino-phenylimino)-(5-methyl-2,3-dihydro-benzofuran-7-yl)-acetonitrile 
• 89-56-5 5-Methylsalicylic acid 
• 22717-57-3 methyl 6-hydroxy-m-toluate 
• 76429-68-0 5-methyl-2,3-dihydrobenzofuran 
• 76429-70-4 7-bromo-5-methyl-2,3-dihydro-benzofuran 
• 99842-50-9 (5-methyl-2,3-dihydro-benzofuran-7-yl)-acetonitrile 
• 33875-89-7 2-methoxy-5-methyl-phenethyl alcohol 
• 103039-08-3 7-chloromethyl-5-methyl-2,3-dihydro-benzofuran 
• 76429-67-9 2-(2,6-Dibromo-4-methylphenoxy)ethyl Bromide 

Downstream Products

• 103261-02-5 5-methyl-2,3-dihydro-benzofuran-7-carbonyl chloride 

Relevant academic research and scientific papers

Zatosetron, a Potent, Selective, and Long-Acting 5HT3 Receptor Antagonist: Synthesis and Structure-Activity Relationships

Antagonists of 5HT3 receptors are clinically effective in treating nausea and emesis associated with certain oncolytic drugs, including cisplatin.Moreover, these agents may be useful in pharmacological management of several central nervous system disorders, including anxiety, schizophrenia, dementia, and substance abuse.Our studies on aroyltropanamides led to the discovery that dihydrobenzofuranyl esters and amides are potent 5HT3 receptor antagonists.Simple benzoyl derivatives of tropine and 3α-aminotropane possessed weak 5HT3 receptor antagonist activity, as judged by blockade of bradycardia produced by iv injection of serotonin (5HT) to anesthetized rats.Within this series, use of benzofuran-7-carboxamide as the aroyl moiety led to a substantial increase of 5HT3 receptor affinity.The optimal 5HT3 receptor antagonist identified via extensive SAR studies was endo-5-chloro-2,3-dihydro-2,2-dimethyl-N-(8-methyl-8-azabicyclooct-3-yl)-7-benzofurancarboxamide (Z)-2-butenedioate (zatosetron maleate).The 7-carbamyl regiochemistry, dimethyl substitution, chloro substituent, and endo stereochemistry were all crucial elements of the SAR.Zatosetron maleate was a potent antagonist of 5HT-induced bradycardia in rats (ED50=0.86 μg/kg iv).Low oral doses of zatosetron (30 μg/kg) produced long-lasting antagonism of 5HT3 receptors, as evidenced by blockade of 5HT-induced bradycardia for longer than 6 h in rats.Moreover, this compound did not produce hemodynamic effects after iv administration to rats, nor did it block carbamylcholine-induced bradycardia in doses that markedly blocked 5HT3 receptors.Thus, zatosetron is a potent, selective, orally effective 5HT3 receptor antagonist with a long duration of action in rats.

CARBOXAMIDES USEFUL AS ANTIEMETIC OR ANTIPSYCHOTIC AGENTS

Carboxamides represented by the formula (I): STR1 wherein Z represents the carbon atoms necessary to complete a 5-to 7-membered ring, R 1, R 2, and R 3 may be the same or different and are selected from the group consisting of a hydrogen atom, a lower alkyl group, a cycloalkyl group, a halogen atom, an amino group, a lower alkylamino group, an alkoxy group, an acylamido group, a sulfonamido group, and a nitro group; andA represents an aminoalkyl moiety and acid addition salts thereof.