FIELD: chemistry.
SUBSTANCE: present invention relates to phenyl substituted pyrrolidones of formula: , where R1 and R5 represent substitutes, which are independently chosen from a group which contains H, CN, halogen, C1-C4alkyl and OR8, where R8 represents C1-C4alkyl, R2 and R4 represent substitutes, which are chosen from a group which contains H, halogen, CN and C1-C4alkyl, R3 represents H, R6 represents a condensed phenyl heterocyclic ring system, chosen from , where R16 represents a substitute, chosen from a group which contains H, C(O)NR18R19 and S(O)2R20, where R18 and R19 represent H or C1-C6alkyl; R20 represents C1-C6alkyl or phenyl; and R17 represents a substitute, which is chosen from a group which contains H, NH2, (CH2)mOH, C(O)NR21R22, SO2R23 and NHSO2R23; where R21 and R22 represent substitutes, which are independently chosen from a group which contains H and substituted or unsubstituted C1-C6alkyl, or, together with a nitrogen atom to which they are bonded, optionally form a ring; R23 represents C1-C6alkyl; and m equals 1; or R6 represents a group, where R9 and R11 represent substitutes, which are independently chosen from a group which contains H, halogen, CN, C(O)NR12R12, NR12R12 and OR12, where each R12 represents H or C1-C4alkyl, and under the condition that, at least one of substitutes R9 and R11 is not hydrogen; R10 represents CN, NR13R14, SO2NHR13, NHSO2R13, O(CH2)nSO2R15, SO2R15, SO2(CH2)nNR13R14 or C(O)NR13R14, where R13 and R14 represent H or C1-C4alkyl; R15 represents C1-C4alkyl, n equals 1-2, and R7 represents halogen, C1-C4alkyl, C2-C4alkenyl or C2-C4alkynyl.
EFFECT: design of compounds and a pharmaceutical composition for inhibiting HIV growth.
19 cl, 12 ex, 1 tbl
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Authors
Dates
2009-10-27—Published
2006-01-30—Filed