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filingDate 1975-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1978-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1498633-A
titleOfInvention 2-phenyl-piperazines and 4-phenyl-hexahydro pyrimidines
abstract 1498633 2-Phenyl-piperazine and 4-phenylhexahydropyrimidine derivatives AKZO NV 28 Jan 1975 [9 Feb 1974] 39732/76 Divided out of 1498632 Heading C2C Novel compounds III and salts thereof in which R 1 and R 2 are H, OH, Hal, C 1-4 alkyl, C 1-4 alkoxy or CF 3 ; R 3 is H, C 1-6 alkyl, C 7-10 aralkyl or amino C 1-6 alkyl in which the amino group is di-C 1-6 alkylated or forms part of a heterocyclic 5- or 6-membered ring; X is OH, Hal, acyloxy or etherified hydroxy; and m = 1 and n = 2 or m = 2 and n = 1; are prepared by reacting a compound VII or a salt thereof in which Y has the same meaning as X except Hal, with (i) Cl-CH 2 COOEt or (COOEt) 2 and reducing the ketone obtained to form compounds III (m = 2, n = 1), (ii) formaldehyde or ClCOOEt and reducing the ketone obtained to form compounds III (m = 1, n=2) or (iii) CH 2 Cl 2 to form compounds III (m = 1, n=2). Compounds III (X = Hal) and (X = acyloxy) are also prepared by halogenating or acylating the corresponding hydroxy compound. Compounds III (m = 2, n = 1) are also prepared by reacting a compound IV or a salt thereof with a compound V or a salt thereof. Compounds IV are prepared by reacting a compound VI or a salt thereof with a dihaloethane, a 1- hydroxy-2-haloethane or ethylene oxide and halogenating any free hydroxy group. Compounds VI are prepared by reacting styrene oxide with an amine R 3 NH 2 . Compounds VII are prepared by reacting a compound VIII or a salt thereof with a compound IX or a salt thereof. Compounds VIII are prepared by halogenating the corresponding α-hydroxy compound.
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Total number of triples: 37.