Method for preparing 6belta-19-oxidosteroids

6b ,19-Oxido-steroids are prepared by treating 6b -hydroxy-10-methyl steroids with an oxidative metal acylate in the presence of iodine and under the influence of a free-radical initiator. Suitable initiators are azo compounds and peroxides, the former preferably having the formula: <FORM:0944268...

Full description

Saved in:
Bibliographic Details
Main Author SZPILFOGEL STEFAN ANTONI
Format Patent
LanguageEnglish
Published 27.10.1964
Subjects
Online AccessGet full text

Cover

Loading…
Abstract 6b ,19-Oxido-steroids are prepared by treating 6b -hydroxy-10-methyl steroids with an oxidative metal acylate in the presence of iodine and under the influence of a free-radical initiator. Suitable initiators are azo compounds and peroxides, the former preferably having the formula: <FORM:0944268/C2/1> (wherein R1 and R2 are hydrogen, or R1, R2, R3 and R4 are the same or different alkyl or aralkyl groups, or R1 and R2 and/or R3 and R4 together form a cycloalkyl group). Suitable acylates are lead tetraacylates and silver and mercury acylates, and the reaction may be performed in an organic solvent to which is preferably added a weak base. Steroids of the androstane, pregnane, cholane, cholestane and spirostane series may be used, particularly important being those saturated in ring A and possibly containing a 5-halogen atom. Examples are given. U.S.A. Specification 3,067,198 is referred to.
AbstractList 6b ,19-Oxido-steroids are prepared by treating 6b -hydroxy-10-methyl steroids with an oxidative metal acylate in the presence of iodine and under the influence of a free-radical initiator. Suitable initiators are azo compounds and peroxides, the former preferably having the formula: <FORM:0944268/C2/1> (wherein R1 and R2 are hydrogen, or R1, R2, R3 and R4 are the same or different alkyl or aralkyl groups, or R1 and R2 and/or R3 and R4 together form a cycloalkyl group). Suitable acylates are lead tetraacylates and silver and mercury acylates, and the reaction may be performed in an organic solvent to which is preferably added a weak base. Steroids of the androstane, pregnane, cholane, cholestane and spirostane series may be used, particularly important being those saturated in ring A and possibly containing a 5-halogen atom. Examples are given. U.S.A. Specification 3,067,198 is referred to.
Author SZPILFOGEL STEFAN ANTONI
Author_xml – fullname: SZPILFOGEL STEFAN ANTONI
BookMark eNrjYmDJy89L5WTQ8U0tychPUUjLL1IoKEotSCzKzEtXMEtKzSlJ1DW01M2vyEzJLy5JLcrPTCnmYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxocHGhqYmpiaGjsaEVQAAuokqiw
ContentType Patent
DBID EVB
DatabaseName esp@cenet
DatabaseTitleList
Database_xml – sequence: 1
  dbid: EVB
  name: esp@cenet
  url: http://worldwide.espacenet.com/singleLineSearch?locale=en_EP
  sourceTypes: Open Access Repository
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Chemistry
Sciences
ExternalDocumentID US3154541A
GroupedDBID EVB
ID FETCH-epo_espacenet_US3154541A3
IEDL.DBID EVB
IngestDate Fri Jul 19 15:14:20 EDT 2024
IsOpenAccess true
IsPeerReviewed false
IsScholarly false
Language English
LinkModel DirectLink
MergedId FETCHMERGED-epo_espacenet_US3154541A3
Notes Application Number: US19620202987
OpenAccessLink https://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19641027&DB=EPODOC&CC=US&NR=3154541A
ParticipantIDs epo_espacenet_US3154541A
PublicationCentury 1900
PublicationDate 19641027
PublicationDateYYYYMMDD 1964-10-27
PublicationDate_xml – month: 10
  year: 1964
  text: 19641027
  day: 27
PublicationDecade 1960
PublicationYear 1964
RelatedCompanies ORGANON INC
RelatedCompanies_xml – name: ORGANON INC
Score 2.3219354
Snippet 6b ,19-Oxido-steroids are prepared by treating 6b -hydroxy-10-methyl steroids with an oxidative metal acylate in the presence of iodine and under the influence...
SourceID epo
SourceType Open Access Repository
SubjectTerms CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
STEROIDS
Title Method for preparing 6belta-19-oxidosteroids
URI https://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19641027&DB=EPODOC&locale=&CC=US&NR=3154541A
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV3dS8MwED_mFPVNpzK_-yB9smjXrGkeiri2Ywj7wG2yt5E0iQ5kLW1F_3yTuKkvewkhgUty8Lu7XHJ3ADfUQynibc_BwpUOalPuBLppMUm8lDFGjSu7P_B7U_Q0a89q8LaOhTF5Qj9NckSFqFThvTLyOv9zYsXmb2V5xxZqKHvoTsLY5j_hYj5S-hLbcSdMRsN4GNlRFE7H9uA59LSpgNzHLdhWRjTWWEheOjomJf-vULoHsDNStJbVIdTEsgF70bruWgN2-6vnbtVdIa88gtu-KfVsKRvTyguhawcuXy2fifeKOi5xsq8F1_EaRbbg5TFcd5NJ1HPUsvPfE86n4_X-vBOoq3u_aILlcox8GeBUqXhEaRpI7BLJfEIkJ_RenEJzE5WzzVPnsK_5pMVvC19AvSo-xKXSqxW7Miz5BqCMfe8
link.rule.ids 230,309,783,888,25576,76876
linkProvider European Patent Office
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwdV3dT8IwEL8gGvFNUYOf7MHsyUXHyro9LEY2lqkMiIDhjbRrp0sMW2BG_3zbCuoLL03TJtf2kt_d9dq7A7giFkoQa1sG5mZqoDZhhiObFk1dK6GUEuXKjvt2NEGP0_a0Am_rWBiVJ_RTJUcUiEoE3kslr4s_J1ag_lYub2gmhvK7cOwFOvsJF7OR0JdYDzpedzgIBr7u-95kpPefPUuaCsi834JtYWBjiYXuS0fGpBT_FUq4DztDQWteHkCFz-tQ89d11-qwG6-eu0V3hbzlIVzHqtSzJmxMrVhwWTtw_qrZlL-XxDBdI__KmIzXWOQZWx5BM-yO_cgQy85-TzibjNb7s46hKu79vAGayTCyUwcnQsUjQhInxaabUtt1U-aSW34CjU1UTjdPNaEWjePerPfQfzqDPckzKYpb-Byq5eKDXwgdW9JLxZ5vsquA4g
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Apatent&rft.title=Method+for+preparing+6belta-19-oxidosteroids&rft.inventor=SZPILFOGEL+STEFAN+ANTONI&rft.date=1964-10-27&rft.externalDBID=A&rft.externalDocID=US3154541A