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filingDate 2017-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fca5c97dd4c46c0c2e8bab709aab98eb
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publicationDate 2018-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-108752-A1
titleOfInvention PROCESS TO CONVERT AN ENANTIOMER S IN ITS RACEMIC FORM
abstract Process to convert the form of the unwanted S enantiomer into its useful racemic form with respect to a 4-aminoindane derivative. Claim 1: A process for the preparation of (R, S) -7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine having the formula (1), starting with (S) -7-Fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine having the formula (2), comprising the steps of: (a) acylating the (S ) -7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine and obtain an indanoamide derivative; (b) oxidizing said indanoamide derivative and obtaining a 3-hydroxyl indanoamide derivative; (c) dehydrate said 3-hydroxyl indanoamide derivative and obtain an indenoamide derivative; (d) deacylate said indenoamide derivative and obtain an indene amine derivative; and (e) hydrogenate said indene amine derivative and obtain the desired (R, S) -7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine. Claim 17: A compound of the formula (3) wherein R is selected from a C₁₋₆ alkyl group or a C₆₋₁₀ aryl group, these groups are optionally substituted with one or more C₁₋₆ alkyl groups and / or atoms of halogen Claim 21: A compound of the formula (4) wherein R is selected from a C₁₋₆ alkyl group or a C₆₋₁₀ aryl group, these groups are optionally substituted with one or more of C₁₋₆ alkyl groups and / or atoms Halogen
priorityDate 2016-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 37.