Organic compounds -- part of the class 532-570 series – Organic compounds – Nitrogen attached directly or indirectly to the purine ring...
Reexamination Certificate
2003-09-02
2009-08-04
Wilson, James O (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Nitrogen attached directly or indirectly to the purine ring...
C544S399000
Reexamination Certificate
active
07569690
ABSTRACT:
If an organic solvent with a water content of 15% or less is used when an oxycarbonyl-substituted piperazine derivative is produced from a piperazine derivative, the piperazine derivative can be oxycarbonylated.
REFERENCES:
patent: 2003/0208074 (2003-11-01), Wu et al.
patent: 2005/0171120 (2005-08-01), Wu et al.
patent: 10-507917 (1998-08-01), None
patent: 2000-7664 (2000-01-01), None
patent: 2001-328938 (2001-11-01), None
patent: WO 96/12492 (1996-05-01), None
Kim, et al., N-Benzyloxycarbonyl-2-methylaminothiazoline as a Selective Benzyloxycarbonylating Reagent of Amines, Bull. Korean Chem. Soc., vol. 24, No. 2, 157-58 (2003).
Bradbury, J.B. et al, “Muscarinic receptor binding and activation of second messengers by substituted N-Methyl-N-[4-(1-azacycloalkyl-2-butnyl]acetamides”,Journal of Medicinal Chemistry, vol. 34, 1991, pp. 1073-1079, XP002437848 US p. 1078, col. 1, paragraph 3.
Steward H.W. et al., “Experimental Chemotherapy of Filariasis, IV The Preparation of Derivatives of Piperazine”,Journal of Organic Chemistry, vol. 13, 1948, pp. 134-143, XPO02437849 US American Chemistry Society, Washington, DC p. 137, procedure (e).
Graham J. Atwell et al., “Monoprotection of χ,ω-Alkanediamines with the N-Benzyloxcarbonyl Group”, Synthesis (Dec. 1984), pp. 1032-1033.
Kazuhiro Kondo et al., “A versatile synthon for chemoselective N-acylation reagents, 2-fluoro-N-mesylaniline”, J. Chem. Soc., Perkin Trans. 1 (1998), pp. 2973-2974.
“Protective Groups in Organic Synthesis,” John Wiley & Sons Inc., Third Edition (1999), pp. 531-532.
“Yukikagaku-Jikken-no-Tebiki 4—Gosei-Hanno”—[II] (English Translation: Introduction to Experiments of Organic Chemistry 4—Synthetic Reactions [II])—(Kagaku Dojin, 1990), with English translation of p. 24, line 17 to p. 25, line 10.
Morimoto Masao
Sato Haruyo
DLA Piper (LLP) US
Leeser Erich A
Toray Fine Chemicals Co., Ltd.
Wilson James O
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