PROBLEM TO BE SOLVED: To obtain a new 3-(condensed ring-substituted) phenyl-5- amidomethyloxazolidinone useful as an antimicrobial agent. SOLUTION: This 3-(condensed ring-substituted) phenyl-5-(amidomethyl) oxazolidin-2-one is shown by formula I [R1 is H, an alkyl, a cycloalkyl, an alkenyl, phenyl, pyridyl, etc.; either R2 or R4 is H and the other and R3 form a group of formula II (n3 and n4 are each 0-3; n7 and n8 are each 0 or 1; R10-1 and R10-2 are each H, an alkyl, etc.; R10-3 and R10-4 are each as shown for R10-1 and R10-2 ), etc.; either R5 or R6 is H and the other is H, an alkyl, etc.], and its pharmaceutically permissible salt such as 3-(1'-oxo-2'-methyl-5'- indanyl)-5-(acetamidomethyl)oxazolidin-2-one. The compound of formula I is prepared by obtaining a compound of formula IV through three processes from a compound of formula III, then forming a compound of formula V, reducing the compound with H2 and further acylating the resulting compound.
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机译:解决的问题:获得新的3-(稠环取代)苯基-5-酰胺基甲基恶唑烷酮作为抗菌剂。解决方案:该3-(稠环取代)苯基-5-(酰胺基甲基)恶唑烷-2-酮由式I表示[R1为H,烷基,环烷基,烯基,苯基,吡啶基等; R 2或R 4为H,另一个与R 3形成式II的基团(n 3和n 4各自为0-3; n 7和n 8各自为0或1; R 10-1和R 10-2各自为H, R10-3和R10-4分别如R10-1和R10-2所示)等。 R5或R6是H,另一个是H,烷基等],及其药学上可接受的盐,例如3-(1'-氧代-2'-甲基-5'-茚满基)-5-(乙酰氨基甲基)恶唑烷-2-酮。式I化合物的制备是通过以下三种方法从式III的化合物获得式IV的化合物,然后形成式V的化合物,将化合物用H 2还原并且进一步酰化所得的化合物。
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