Forms of cabergoline

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C514S288000, C546S067000

Reexamination Certificate

active

07026483

ABSTRACT:
The invention provides methods for preparing amorphous physical form of cabergoline, and solvate form A of cabergoline useful in the preparation of the first mentioned physical form. A method for treating a prolactin disorder with medicaments prepared from amorphous physical form of cabergoline and solvate form A of cabergoline is also disclosed.

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patent: 6673806 (2004-01-01), Tomasi et al.
patent: 6680327 (2004-01-01), Candiani et al.
patent: 6696568 (2004-02-01), Gutman et al.
patent: 2002/0123503 (2002-09-01), Ross et al.
patent: 2003/0149067 (2003-08-01), Tomasi et al.
patent: 2103603 (1983-02-01), None
patent: WO 01/70740 (2001-09-01), None
patent: WO 03/78392 (2003-09-01), None
patent: WO 03/78433 (2003-09-01), None
Ashford, S., et al., “A Practical Synthesis of Cabergoline,”J. Org. Chem.,67: 7147-50, 2002.
Brambilla, E., et al., “Synthesis and Nidation Inhibitory Activity of a New Class of Ergoline Derivatives,”Eur. J. Med. Chem.,24: 421-26, 1989.
Candiani, I., et al., “The Ligand Effect in Copper(I)-Catalyzed Chemoselective Amide Carbamoylation in Cabergoline Synthesis,”Synlett,605-06, 1995.
Sabatino, P., et al., “X-ray Crystal Structure and Conformational Analysis of N-(3-Dimetylaminopropyl)-N-(Ethylaminocarbonyl)-6-(2-propenyl)Ergoline-8β-Carboxamide (Cabergoline): Comparison with Bromocriptine and Lisuride and a Hypothesis for its High Dopaminergic Activity,”Il Farmaco,50: 175-78, 1995.
Federal Register, 62: 67377-88, 1997.
The Merck Index, 12thEdition, p. 1637, 1996.

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