http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016030704-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 2015-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2daedcfd4e4d4943a9eb19937315b13
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publicationDate 2016-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2016030704-A1
titleOfInvention Solid form of intermediate of ticagrelor
abstract A process for the preparation of a solid form of a compound of formula (VII) (Formula (VII)) comprises coupling(1 R ,2 S )-2-(3,4-difluorophenyl)cyclopropanamine (R)-Mandelic acid of Formula (VI) with (2-[[(3a R ,4 S ,6 R ,6aS)-6-[7-chloro-5-(propylthio)-3 H -1,2,3-triazolo[4,5- d ]pyrimidin-3-yl]-2,2- dimethyltetrahydro-3a H -cyclopenta[d[[1,3]dioxol-4-yl]oxy]-1-ethanol) of formula (V) in the presence of a suitable base and a first a suitable solvent at a suitable temperature to form 2- [[(3aR,4S,6R,6aS)-6-[7-[[(1R,2S)-2-(3,4-difluorophenyl)cyclopropyl]amino]-5-(propylthio)-3H-1,2,3- triazolo[4,5-d]pyrimidin-3-yl]-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy]-1- ethanol of formula (VI)I; and isolating the compound of formula (VII) using a second suitable solvent so as to produce the compound of formula (VII) in solid form. A process for preparing Ticagrelor of formula (I) or a salt thereof (Formula (I)) comprises the conversion of a compound of formula (VII) in a solid form either as free base or as an acid addition salts thereof, into a compound of formula (I).
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