Optically active 1-(fluoro-, trifluoromethyl-or...

Organic compounds -- part of the class 532-570 series – Organic compounds – Amino nitrogen containing

Reexamination Certificate

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C564S304000

Reexamination Certificate

active

10476650

ABSTRACT:
An optically active 1-(fluoro-, trifluoromethyl- or trifluoromethoxy-substituted phenyl)alkylamine N-monoalkyl derivative represented by the formula 4 is produced by a process including (a) reacting an optically active secondary amine, represented by the formula 1, with an alkylation agent R2—X, in the presence of a base, thereby converting the secondary amine into an optically active tertiary amine represented by the formula 3; and (b) subjecting the tertiary amine to a hydrogenolysis, thereby producing the N-monoalkyl derivative,wherein R represents a fluorine atom, trifluoromethyl group or trifluoromethoxy group, n represents an integer of from 1 to 5, each of R1and R2independently represents an alkyl group having a carbon atom number of from 1 to 6, Me represents a methyl group, Ar represents a phenyl group or 1- or 2-naphthyl group, * represents a chiral carbon, and X represents a leaving group.

REFERENCES:
patent: 2002/0103400 (2002-08-01), Ishii et al.
patent: 2003/0028021 (2003-02-01), Alvaro et al.
patent: 01/25219 (2001-04-01), None
patent: 02/32867 (2002-04-01), None
patent: WO 02/32867 (2002-04-01), None
U.S. Appl. No. 10/422,652, filed May 21, 2003, Ishii et al.
Posner et al., “Methyl and n-Alkyl Ketones from Carboxylic Acid Chlorides and Organocopper Reagents”Tetrahedron Letters, No. 53, (1970) pp. 4647-4650.
Chemical Journal of Chinese Universities, Feb. 9, 1988, vol. 9, No. 2, pp. 134-139.
Gilbert, A., et al., “Excited State Substitution and Addition Reactions of Aryl Fluorides with Aliphatic Amines,” Department of Chemistry, University of Reading, pp. 1393-1399, Jul. 1980.
Japanese Office Action dated Jun. 16, 2006 and an English translation thereof (Eight (8) pages).
Correspondence dated Jul. 28, 2006, (Two (2) pages).

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