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US3994875A Expired / Lapsed US ⏱️ 0.0 years remaining

Antibiotics

Assignee: Yeda Research and Development Co Ltd
•
Filing: 1975-12-16
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Granted: 1976-11-30
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Expires: 1995-12-16
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Abstract

Abstract Novel cephalosporin and penicillin antibiotic derivatives.

Inventors

  • 👤 Abraham Patchornik
  • 👤 Fortuna Haviv

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 09:38
CPC Classifications
C; C07; C07D; C07D499/00

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 366 words
A compound selected from a base of the formula ##SPC14## wherein Aryl is selected from phenyl or 2-thienyl; Y is selected from hydrogen, chlorine, bromine, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, or an alkoxy group of from 1 to 4 carbon atoms with the proviso that when Aryl is 2-thienyl, Y is hydrogen; each of R 1 , R 2 and R 3 is selected from hydrogen or a straight or branched lower alkyl group of from 1 to 4 carbon atoms; Z is selected from a bond, oxygen, sulfur or imino with the proviso that when Aryl is 2-thienyl, Z is a bond; W is selected from hydrogen, methyl, anino, hydroxy, SO 3 H, or COOR 4 wherein R 4 is selected from hydrogen or 5-indanyl; n is zero, 1 or 2 with the proviso that when W is other than hydrogen or methyl and Z is other than a bond, n is not zero; R 5 is selected from hydrogen or methoxy; M is selected from hydrogen, a pharmaceutically acceptable non-toxic cation charge, an alkanoyloxymethyl group wherein the alkanoyl moiety has from 1 to 5 carbon atoms and may be straight or branched, an alkanoylaminomethyl group wherein the alkanoyl moiety has from 1 to 5 carbon atoms and may be straight or branched and wherein the amino nitrogen may be substituted with an alkyl group of from 1 to 4 carbon atoms, an alkoxycarbonylaminomethyl group wherein the alkoxy moiety has from 1 to 4 carbon atoms and may be straight or branched and wherein the amino nitrogen may be substituted with an alkyl group of from 1 to 4 carbon atoms, p-(alkanoyloxy)benzyl wherein the alkanoyl moiety contains from 1 to 5 carbon atoms and may be straight or branched or aminoalkanoyloxymethyl as represented by the group ##EQU1## wherein n' is 0 to 5, each of R 11 and R 12 is selected from hydrogen or lower alkyl of from 1 to 4 carbon atoms, and each of R 13 and R 14 is selected from hydrogen or a straight or branched lower alkyl group of from 1 to 4 carbon atoms; and pharmaceutically acceptable salts thereof.
Claim 2
Dependent Claim 366 words
A compound selected from a base of the formula ##SPC14## wherein Aryl is selected from phenyl or 2-thienyl; Y is selected from hydrogen, chlorine, bromine, a straight or branched lower alkyl group of from 1 to 4 carbon atoms, or an alkoxy group of from 1 to 4 carbon atoms with the proviso that when Aryl is 2-thienyl, Y is hydrogen; each of R 1 , R 2 and R 3 is selected from hydrogen or a straight or branched lower alkyl group of from 1 to 4 carbon atoms; Z is selected from a bond, oxygen, sulfur or imino with the proviso that when Aryl is 2-thienyl, Z is a bond; W is selected from hydrogen, methyl, anino, hydroxy, SO 3 H, or COOR 4 wherein R 4 is selected from hydrogen or 5-indanyl; n is zero, 1 or 2 with the proviso that when W is other than hydrogen or methyl and Z is other than a bond, n is not zero; R 5 is selected from hydrogen or methoxy; M is selected from hydrogen, a pharmaceutically acceptable non-toxic cation charge, an alkanoyloxymethyl group wherein the alkanoyl moiety has from 1 to 5 carbon atoms and may be straight or branched, an alkanoylaminomethyl group wherein the alkanoyl moiety has from 1 to 5 carbon atoms and may be straight or branched and wherein the amino nitrogen may be substituted with an alkyl group of from 1 to 4 carbon atoms, an alkoxycarbonylaminomethyl group wherein the alkoxy moiety has from 1 to 4 carbon atoms and may be straight or branched and wherein the amino nitrogen may be substituted with an alkyl group of from 1 to 4 carbon atoms, p-(alkanoyloxy)benzyl wherein the alkanoyl moiety contains from 1 to 5 carbon atoms and may be straight or branched or aminoalkanoyloxymethyl as represented by the group ##EQU1## wherein n' is 0 to 5, each of R 11 and R 12 is selected from hydrogen or lower alkyl of from 1 to 4 carbon atoms, and each of R 13 and R 14 is selected from hydrogen or a straight or branched lower alkyl group of from 1 to 4 carbon atoms; and pharmaceutically acceptable salts thereof.
Claim 3
Dependent Claim 9 words
A compound of claim 1 wherein W is hydrogen.
Claim 4
Dependent Claim 10 words
A compound of claim 2 wherein Z is a bond.
Claim 5
Dependent Claim 11 words
A compound of claim 2 wherein Z is oxygen or sulfur.
Claim 6
Dependent Claim 9 words
A compound of claim 2 wherein Z is imino.
Claim 7
Dependent Claim 9 words
A compound of claim 1 wherein W is methyl.
Claim 8
Dependent Claim 10 words
A compound of claim 6 wherein Z is a bond.
Claim 9
Dependent Claim 11 words
A compound of claim 6 wherein Z is oxygen or sulfur.
Claim 10
Dependent Claim 9 words
A compound of claim 6 wherein Z is imino.
Claim 11
Dependent Claim 9 words
A compound of claim 1 wherein W is hydroxy.
Claim 12
Dependent Claim 10 words
A compound of claim 10 wherein Z is a bond.
Claim 13
Dependent Claim 11 words
A compound of claim 10 wherein Z is oxygen or sulfur.
Claim 14
Dependent Claim 9 words
A compound of claim 10 wherein Z is imino.
Claim 15
Dependent Claim 9 words
A compound of claim 1 wherein W is amino.
Claim 16
Dependent Claim 10 words
A compound of claim 14 wherein Z is a bond.
Claim 17
Dependent Claim 11 words
A compound of claim 14 wherein Z is oxygen or sulfur.
Claim 18
Dependent Claim 9 words
A compound of claim 14 wherein Z is imino.
Claim 19
Dependent Claim 14 words
A compound of claim 1 wherein W is COOR 4 or SO 3 H.
Claim 20
Dependent Claim 10 words
A compound of claim 18 wherein Z is a bond.
Claim 21
Dependent Claim 11 words
A compound of claim 18 wherein Z is oxygen or sulfur.
Claim 22
Dependent Claim 9 words
A compound of claim 18 wherein Z is imino.

References Cited (Backward Citations)

BE753387A Cited
DE2203653A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-11-30 1980-05-31 1980-11-30 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-11-30 1984-05-31 1984-11-30 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-11-30 1988-05-31 1988-11-30 $7700.00 Window Closed / Lapsed

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