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US2493780A Expired / Lapsed US ⏱️ 0.0 years remaining

3,11-diketo-17,20-dihydroxypregnanes and process

Assignee: Merck and Co Inc
•
Filing: 1946-07-13
•
Granted: 1950-01-10
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Expires: 1966-07-13
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Abstract

No abstract record available.

Inventors

  • 👤 Sarett Lewis Hastings

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-03 14:05
CPC Classifications
C; C07; C07J; C07J5/00; C07J75/00

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 121 words
THE PROCESS OF PREPARING 3,11-DIKETO-17,20DIHYDROXY PREGNANE IN SUBSTANTIALLY PURE FORM, WHICH COMPRISES REACTING A MIXTURE CONTAINING $**17,20-3,11-DIKETO-PREGNANE AND $**20,21-3,11-DIKETOPREGNANE WITH A COMPOUND SELECTED FROM THE CLASS WHICH CONSISTS OF OSMIUM TETROXIDE AND HYDROGEN PEROXIDE TO PRODUCE A MIXTURE CONTAINING 3,11-DIKETO-17,20-DIHYDROXY PREGNANE, 3,11DIKETO- 20 - ALPHA - 21 DITHYDROXY PREGNANE, AND 3,11-DIKETO-20-BETA-21-HYDROXY-PREGNANE; REACTING THIS MIXTURE WITH A CYCLIC ANHYDRIDE OF A DICARBOXYLIC ACID TO CONVERT THE 20,21-DIHYDROXY CARBOXYLIC ACID TO CONVERT THE 20,21-DIHYDROXY STEREOISOMERS TO THE CORRESPONDING STEROISOMERS OF 3,11-DIKETO-20-HYDROXY-21-(CARBOXY-ACYLOXY) PREGNANE ADMIXED WITH UNCHANGED 3,11-DIKETO17,20-DIHYDROXY-PREGNANE; SEPARATING THE NONACIDIC 3,11-DIKETO-17,20-DIHYDROXY PREGNANE FROM THIS MIXTURE; REACTING THIS COMPOUND WITH AN ACYLATING AGENT TO PRODUCE 3,11-DIKETO-17-HYDROXY-20-ACYLOXY-PREGNANE; PURIFYING THIS ACYLOXY DERIVATIVE BY FRACTIONAL CRYSTALLIZATION; AND HYDROLYZING TO PRODUCE THE DESIRED 3,11-DIKETO17,20-DIHYDROXY PREGNANE IN SUBSTANTIALLY PURE FORM.
Claim 2
Dependent Claim 121 words
THE PROCESS OF PREPARING 3,11-DIKETO-17,20DIHYDROXY PREGNANE IN SUBSTANTIALLY PURE FORM, WHICH COMPRISES REACTING A MIXTURE CONTAINING $**17,20-3,11-DIKETO-PREGNANE AND $**20,21-3,11-DIKETOPREGNANE WITH A COMPOUND SELECTED FROM THE CLASS WHICH CONSISTS OF OSMIUM TETROXIDE AND HYDROGEN PEROXIDE TO PRODUCE A MIXTURE CONTAINING 3,11-DIKETO-17,20-DIHYDROXY PREGNANE, 3,11DIKETO- 20 - ALPHA - 21 DITHYDROXY PREGNANE, AND 3,11-DIKETO-20-BETA-21-HYDROXY-PREGNANE; REACTING THIS MIXTURE WITH A CYCLIC ANHYDRIDE OF A DICARBOXYLIC ACID TO CONVERT THE 20,21-DIHYDROXY CARBOXYLIC ACID TO CONVERT THE 20,21-DIHYDROXY STEREOISOMERS TO THE CORRESPONDING STEROISOMERS OF 3,11-DIKETO-20-HYDROXY-21-(CARBOXY-ACYLOXY) PREGNANE ADMIXED WITH UNCHANGED 3,11-DIKETO17,20-DIHYDROXY-PREGNANE; SEPARATING THE NONACIDIC 3,11-DIKETO-17,20-DIHYDROXY PREGNANE FROM THIS MIXTURE; REACTING THIS COMPOUND WITH AN ACYLATING AGENT TO PRODUCE 3,11-DIKETO-17-HYDROXY-20-ACYLOXY-PREGNANE; PURIFYING THIS ACYLOXY DERIVATIVE BY FRACTIONAL CRYSTALLIZATION; AND HYDROLYZING TO PRODUCE THE DESIRED 3,11-DIKETO17,20-DIHYDROXY PREGNANE IN SUBSTANTIALLY PURE FORM.

References Cited (Backward Citations)

US2183589A Cited
FR816852A Cited
US2254562A Cited
US2265143A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1953-01-09 1953-07-11 1954-01-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1957-01-09 1957-07-11 1958-01-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1961-01-09 1961-07-11 1962-01-10 $7700.00 Window Closed / Lapsed

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