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Antibiotics steffimycinol and 7-deoxysteffimycinol and process for preparing the same

Assignee: Pharmacia and Upjohn Co
•
Filing: 1977-03-09
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Granted: 1978-05-16
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Expires: 1997-03-09
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Abstract

Abstract Antibiotics steffimycinol and 7-deoxysteffimycinol produced by reduction of the antibiotic steffimycinone. Steffimycinol is active against various microorganisms, for example, Bacillus subtilis, Mycobacterium avium and Streptococcus pyogenes; 7-deoxysteffimycinol is active against Sarcina lutea, Bacillus cereus, and B. subtilis. Thus, these antibiotics can be used to inhibit the growth of the above microorganisms in various environments.

Inventors

  • 👤 James M. Koert
  • 👤 Paul F. Wiley

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 10:53
CPC Classifications
C; C07; C07C; C07C46/00

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 16 words
Steffimycinol, a compound having the following structure: ##STR3## and alkali and alkaline earth metal salts thereof.
Claim 2
Dependent Claim 16 words
Steffimycinol, a compound having the following structure: ##STR3## and alkali and alkaline earth metal salts thereof.
Claim 3
Dependent Claim 16 words
7-Deoxysteffimycinol, a compound having the following structure: ##STR4## and alkali and alkaline earth metal salts thereof.
Claim 4
Dependent Claim 16 words
7-Deoxysteffimycinol, a compound having the following structure: ##STR4## and alkali and alkaline earth metal salts thereof.
Claim 5
Dependent Claim 48 words
Tetra-O-acylates of the compound defined in claim 1 wherein said acyl group consists of a hydrocarbon carboxylic acid acyl of from 2 to 18 carbon atoms, inclusive; halo-, nitro-, hydroxy-, amino-, cyano-, thiocyano-, and lower alkoxy-substituted hydrocarbon carboxylic acid acyl of from 2 to 18 carbon atoms, inclusive.
Claim 6
Dependent Claim 48 words
Tri-O-acylates of the compound defined in claim 2 wherein said acyl group consists of a hydrocarbon carboxylic acid acyl of from 2 to 18 carbon atoms, inclusive; halo-, nitro-, hydroxy-, amino-, cyano-, thiocyano-, and lower alkoxy-substituted hydrocarbon carboxylic acid acyl of from 2 to 18 carbon atoms, inclusive.
Claim 7
Dependent Claim 26 words
A process for preparing the compound of claim 1 which comprises reduction of steffimycinone with one mole or less of a metal hydride or aluminum isopropoxide.
Claim 8
Dependent Claim 13 words
A process, according to claim 5, wherein NaBH 4 is the metal hydride.
Claim 9
Dependent Claim 21 words
A process, according to claim 5, wherein one mole or less of the metal hydride is used per mole of steffimycinone.
Claim 10
Dependent Claim 25 words
A process for preparing the compound of claim 2 which comprises reduction of steffimycinone with a large excess of a metal hydride or aluminum isopropoxide.
Claim 11
Dependent Claim 13 words
A process, according to claim 8, wherein NaBH 4 is the metal hydride.
Claim 12
Dependent Claim 20 words
A process, according to claim 8, wherein about 5 moles of the metal hydride is used per mole of steffimycinone.

References Cited (Backward Citations)

US3590028A Cited
US3803124A Cited
US3665018A Cited
US3721684A Cited
US3976667A Cited
US4021457A Cited
US4012448A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-05-15 1981-11-14 1982-05-16 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-05-15 1985-11-14 1986-05-16 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-05-15 1989-11-14 1990-05-16 $7700.00 Window Closed / Lapsed

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