Method for producing cyclic diamine derivative or salt thereof

Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...

Reexamination Certificate

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C544S242000, C544S358000

Reexamination Certificate

active

07459552

ABSTRACT:
The present invention is directed to a method for producing a cyclic diamine compound (3) or a salt thereof through the following scheme:(wherein Ar represents a phenyl group, a pyridyl group, or a pyrimidinyl group, any of which may have a substituent; X represents NH, S, or O; ring A represents a benzene ring or a pyridine ring, which may have a substituent; 1 represents an integer of 1 or 2; m represents an integer of 1 or 2; and n represents an integer of 1 to 6). The method enables synthesis of a cyclic diamine compound (3) or a salt thereof, which serves as an ACAT inhibitor, in an industrially useful manner.

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patent: 2005/0020606 (2005-01-01), Shibuya et al.
patent: 2006/0293519 (2006-12-01), Shibuya et al.
U.S. Appl. No. 10/558,197, filed Nov. 25, 2005, Shibuya, et al.
U.S. Appl. No. 10/535,705, filed May 20, 2005, Shibuya et al.
Kubota, Toshio et al., Facile Synthesis of Unsymmetrical Sulfides Using Bis (2,2,2-Trifluoroethoxy) Triphenylphosphorane, Chemistry LettersNo. 7, pp. 845-846, 1979.
Vader, Jan et al., Stereoselective Syntheses of 2-Substituted Perhydrofuro (2, 3-b) furans, Tetrahedron, vol. 44, No. 9, pp. 2663-2674, 1988.
U.S. Appl. No. 11/631,397, filed Dec. 29, 2006, Shibuya et al.

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