发明名称 PROCESS FOR OBTAINING PYRAZINE DERIVATIVES
摘要 Pyrazine derivatives by the formula <IMAGE> are disclosed. In the above formula, R1 and R2, which may be the same or different, each represents a hydrogen atom, a halogen atom, a hydroxy group, a lower alkoxy group, a phenyl lower alkoxy group, a phenoxy group, a mercapto group, a lower alkylthio group, a phenyl lower alkylthio group, a phenylthio group, an amino group, a substituted amino group, a lower alkyl group, a carbamoyl group or a sulfamoyl group; R3 represents a lower alkoxy group; R4, R5, and R6, which may be the same or different, each represents a hydrogen atom, a lower alkyl group, a cycloalkyl group, a phenyl lower alkyl group, or a phenyl group; and A represents a lower alkylene group; said R4 and A, said R5 and A, said R4 and R5, or said R5 and R6 may form a 5-membered or 6-membered nitrogen-containing heterocyclic ring which may further contain a hetero-atom together with nitrogen atom, and the pharmacologically acceptable non-toxic salts thereof. The compounds of this invention have a strong and selective antiematic activity and an effect of stimulating the gastric motility.
申请公布号 YU347074(A) 申请公布日期 1982.06.18
申请号 YU19740003470 申请日期 1974.12.26
申请人 YAMANOUCHI PHARMACEUTICAL CO LTD 发明人 MARAKAMI MASUO;TAKAHASHI KOZO;HIRATA YASUHUMI;TAKASHIMA MUTSUO;TAKEDA MASAAKI;INO HIROYOSCHI;IWANAMI SUMIO
分类号 C07D241/24;C07D241/28 主分类号 C07D241/24
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