Document Type and Number:
Japanese Patent JPS5017992
Kind Code:
B1
Abstract:
1333222 Amidinothiocephalosporins; thiourea derivatives BRISTOL-MYERS CO 29 Oct 1970 [30 Oct 1969] 51543/70 Headings C2A and C2C Novel cephaolsporins having the Formula I wherein A is hydrogen, C 2 to C 8 alkanoyloxy, azido, benzoyloxy or a quaternary ammonium radical, M is hydrogen, a non-toxic cation or an anionic charge when A is quaternary ammonium, and R, R1 and R2 are C 1 to C 7 alkyl, C 2 to C 6 alkenyl, C 2 to C 6 alkynyl or C 3 to C 7 cycloalkyl and R2 may also be hydrogen, and non-toxic acid addition salts thereof in which M is hydrogen are prepared by reacting a corresponding 7-amino-cephalosporanic acid or salt thereof with an acid halide of formula wherein Hal is Cl, Br or I and X is Cl, Br or I or a group of formula in which R, R 1 and R 2 are as previously defined, or with an N-acylating functional equivalent of such an acid halide and, when X is C1, Br or I, reacting the resulting intermediate of Formula X with a compound of Formula XI wherein R, R 1 and R 2 are as previously defined. The preferred acylating agent is bromoacetyl bromide. Functional equivalents may be the acid anhydride or mixed anhydrides with another acid. The intermediate (X) may be isolated as its salt (e.g. Na or K) or as the free haloacetamidocephalosporanic acid. Compounds of Formula XI (above) are prepared by reacting an appropriate primary or secondary amine (i.e. primary when R2 is H, secondary when R2 is other than H) with R- isothiocyanate. Pharmaceutical compositions having antibiotic activity against gram-positive and -negative bacteria comprise a cephalosporin of Formula I or a non-toxic acid-addition salt thereof together with a pharmaceutically acceptable carrier.
Application Number:
JP9480970A
Publication Date:
June 25, 1975
Filing Date:
October 29, 1970
Export Citation:
International Classes:
C07D501/28; A23K20/195; C07C335/08; C07D501/20; C07D501/40; (IPC1-7): C07D501/26; C07D501/38