US 5,708,169 A · 5-amidomethyl .alpha.,.beta.-saturated and -unsaturated 3-aryl butyrolactone antibacterial agents

Abstract

The present invention provides for new 5-amidomethyl, .alpha.,.beta.-saturated and--unsaturated butyrolactone antibacterial agents of formula I ##STR1## characterized by 3-aryl substituents that include, for example, indolinyl and phenyl substituted with zero (0) to two(2) halogen atoms and substituted in the para position with, e.g., piperazinyl, thiomorpholinyl (and corresponding sulfoxide and sulfone), thiazolidinyl (and sulfoxide and sulfone), morpholinyl, azetidinyl, pyrrolidinyl, piperidinyl, pyrrolyl, azepinyl, troponyl, 3,7-diazabicyclo3.3.0!octan-3-yl, bridged thiazinyl or bridged oxazinyl moieties. In those cases where a ring nitrogen is present, then this is substituted to form an amide, formamide, sulfonamide, urethane, or alkylated with a wide variety of moieties. These compounds are effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria such as multiply-resistant staphylococci, streptococci and enterococci, as well as anaerobic organisms such as Bacteroides spp. and Clostridia spp. species, and acid-fast organisms such as Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp., and in organisms such as Mycoplasma spp.

A compound of the formula I

wherein --- is a single or double bond;
wherein X.sup.1 and X.sup.2 are independently
--H,
--F, or
--Cl;
wherein Q.sup.1 is:
##STR36## Q.sup.1 and X.sup.2 taken together are ##STR37## wherein Z.sup.1 is a) --CH.sub.2 --,
b) --CH(R.sup.4)--CH.sub.2 --,
c) --C(O)--, or
d) --CH.sub.2 CH.sub.2 CH.sub.2 --;
wherein Z.sup.2 is
a) --O.sub.2 S--,
b) --O--,
c) --N(R.sup.7)--,
d) --OS--, or
e) --S--;
wherein Z.sup.3 is
a) --O.sub.2 S--,
b) --O--,
c) --OS--, or
d) --S--;
wherein A.sup.1 is
a) H--, or
b) CH.sub.3 ;
wherein A.sup.2 is
a) H--,
b) HO--,
c) CH.sub.3 --,
d) CH.sub.3 O--,
e) R.sup.2 O--CH.sub.2 --C(O)--NH--
f) R.sup.3 O--C(O)--NH--,
g) (C.sub.1 -C.sub.2)alkyl-O--C(O)--,
h) HO--CH.sub.2 --,
i) CH.sub.3 O--NH--,
j) (C.sub.1 -C.sub.3)alkyl-O.sub.2 C--
k) CH.sub.3 --C(O)--,
l) CH.sub.3 --C(O)--CH.sub.2 --, ##STR38## A.sup.1 and A.sup.2 taken together are:
##STR39## wherein R.sup.1 is a) --CHO,
b) --COCH.sub.3,
c) --COCHCl.sub.2,
d) --COCHF.sub.2,
e) --CO.sub.2 CH.sub.3,
f) --SO.sub.2 CH.sub.3, or
g) --COCH.sub.2 OH;
wherein R.sup.2 is
a) H--,
b) CH.sub.3 --,
c) phenyl-CH.sub.2 --, or
d) CH.sub.3 C(O)--;
wherein R.sup.3 is
a) (C.sub.1 -C.sub.3)alkyl-, or
b) phenyl-;
wherein R.sup.4 is
a) H--, or
b) HO--;
wherein R.sup.5 is
a) H--,
b) (C.sub.1 -C.sub.3)alkyl-,
c) CH.sub.2 .dbd.CH--CH.sub.2 --, or
d) CH.sub.3 --O--(CH.sub.2).sub.2 --;
wherein R.sup.6 is
a) CH.sub.3 --C(O)--,
b) H--C(O)--,
c) Cl.sub.2 CH--C(O)--,
d) HOCH.sub.2 --C(O)--,
e) CH.sub.3 SO.sub.2 --, ##STR40## g) F.sub.2 CHC(O)--, ##STR41## i) H.sub.3 C--C(O)--O--CH.sub.2 --C(O)--, j) H--C(O)--O--CH.sub.2 --C(O)--, ##STR42## l) HC.tbd.C--CH.sub.2 O--CH.sub.2 --C(O)--, or m) phenyl-CH.sub.2 --O--CH.sub.2 --C(O)--;
wherein R.sup.7 is
a) R.sup.2 O--C(R.sub.10)(R.sub.11)--C(O)--,
b) R.sup.3 O--C(O)--,
c) R.sup.8 --C(O)--, ##STR43## f) H.sub.3 C--C(O)--(CH.sub.2).sub.2 --C(O)--, g) R.sup.9 --SO.sub.2 --, ##STR44## i) HO--CH.sub.2 --C(O)--, j) R.sup.16 --(CH.sub.2).sub.2 --,
k) R.sup.13 --C(O)--O--CH.sub.2 --C(O)--,
l) (CH.sub.3).sub.2 N--CH.sub.2 --C(O)--NH--,
m) NC--CH.sub.2 --, or
n) F.sub.2 --CH--CH.sub.2 --;
wherein R.sup.8 is
a) H--,
b) (C.sub.1 -C.sub.4)alkyl,
c) aryl --(CH.sub.2).sub.p,
d) ClH.sub.2 C--,
e) Cl.sub.2 HC--,
f) FH.sub.2 C--,
g) F.sub.2 HC--, or
h) (C.sub.3 -C.sub.6)cycloalkyl;
wherein R.sup.9 is
a) --CH.sub.3,
b) --CH.sub.2 Cl
c) --CH.sub.2 CH.dbd.CH.sub.2,
d) aryl, or
e) --CH.sub.2 CN;
wherein R.sup.10 and R.sup.11 are independently
a) H--,
b) CH.sub.3 --;
or
wherein R.sup.12 is
a) H--,
b) CH.sub.3 O--CH.sub.2 O--CH.sub.2 --, or
c) HOCH.sub.2 --;
wherein R.sup.13 is
a) CH.sub.3 --,
b) HOCH.sub.2 --,
c) (CH.sub.3).sub.2 N-phenyl, or
d) (CH.sub.3).sub.2 N--CH.sub.2 --;
wherein R.sup.14 is
a) HO--,
b) CH.sub.3 O--,
c) H.sub.2 N--,
d) CH.sub.3 O--C(O)--O--,
e) CH.sub.3 --C(O)--O--CH.sub.2 --C(O)--O--,
f) phenyl-CH.sub.2 --O--CH.sub.2 --C(O)--O--,
g) HO--(CH.sub.2).sub.2 --O--,
h) CH.sub.3 O--CH.sub.2 --O--(CH.sub.2).sub.2 --O--, or
i) CH.sub.3 O--CH.sub.2 --O--;
wherein R.sup.15 is
a) H--, or
b) Cl--;
wherein R.sup.16 is
a) HO--
b) CH.sub.3 O--, or
c) F;
wherein m is zero (0) or one (1);
wherein n is one (1) to three (3), inclusive;
wherein p is zero (0) or one (1);
wherein aryl is phenyl substituted with zero (0) or one (1) of the following:
a) --F,
b) --Cl,
c) --OCH.sub.3,
d) --OH,
e) --NH.sub.2,
f) --(C.sub.1 -C.sub.4)alkyl,
g) --O--C(O)--OCH.sub.3, or
h) --NO.sub.2 ;
or pharmaceutically acceptable salts thereof.

129 more elements

5-amidomethyl .alpha.,.beta.-saturated and -unsaturated 3-aryl butyrolactone antibacterial agents

Life of this patent

5-amidomethyl .alpha.,.beta.-saturated and -unsaturated 3-aryl butyrolactone antibacterial agents

Life of this patent

Abstract

Claims9