http://rdf.ncbi.nlm.nih.gov/pubchem/patent/MX-348917-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4d3f1bfec8ac94cca9554e3c17db5c6d
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J1-0066
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J75-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07J51-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07J75-00
filingDate 2012-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a46f594b1e0239d5ea128f9270b0e2be
publicationDate 2017-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber MX-348917-B
titleOfInvention PROCESS FOR THE PRODUCTION OF ESTETROL.
abstract The present invention relates to a process for the preparation of a compound of the formula (I), hydrates or solvents thereof; (I) such a process comprises the steps of (a) reacting a compound of the formula (II) with an acylating agent and a silylating agent to produce a compound of the formula (III), (II) (III) in where P1 is a protective group selected from R1CO-, or R2Si (R3) (R4) -, P2 is a protective group selected from (R6R5R7) C-CO-, or (R2) Si (R3) (R4) -, in wherein R1 is a group selected from C1-6alkyl or C3-6cycloalkyl, each group is optionally substituted by one or more substituents independently selected from fluorine or C1-4alkyl; R2, R3 and R4 are each independently a group selected from C1-6alkyl or phenyl, each group is optionally substituted by one or more substituents independently selected from fluorine or C1-4alkyl; R5 is a group selected from C1-6alkyl or phenyl, each group is optionally substituted by one or more substituents independently selected from fluorine or C1-4alkyl; R6 and R7 are each independently hydrogen or a group selected from C1-6alkyl or phenyl, each group is optionally substituted by one or more substituents independently selected from fluorine or C1-4alkyl; b) reacting the compound of the formula (III) in the presence of at least one oxidizing agent selected from a permanganate salt, osmium oxide, hydrogen peroxide or iodine and silver acetate to produce a compound of the formula (IV) ; and (IV) 5 c) Deprotect the compound of the formula (IV) to produce the compound of the formula (I).
priorityDate 2011-10-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 28.