Process for producing crystal

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

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

Reexamination Certificate

active

07569696

ABSTRACT:
The present invention relates to a production method of a crystal of (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]benzimidazole.n′H2O (wherein n′ is about 0 to about 0.1) or a salt thereof, which characteristically includes crystallization from an organic solvent solution or suspension in which (R)-2-[[[3-methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-benzimidazole.nH2O (wherein n is about 0.1 to about 1.0) or a salt thereof has been dissolved or suspended, and the like, and provides a convenient method for efficiently producing an optically active sulfoxide derivative having an extremely high enantiomer excess in high yield at an industrial large scale.

REFERENCES:
patent: 4628098 (1986-12-01), Nohara et al.
patent: 6002011 (1999-12-01), Kato et al.
patent: 6462058 (2002-10-01), Fujishima et al.
patent: 6664276 (2003-12-01), Fujishima et al.
patent: 1223262 (1999-07-01), None
patent: 0174726 (1986-03-01), None
patent: 0302720 (1989-02-01), None
patent: 1191025 (2002-03-01), None
patent: WO 92/08716 (1992-05-01), None
patent: WO 96/02535 (1996-02-01), None
patent: WO 9602535 (1996-02-01), None
patent: WO 96/17077 (1996-06-01), None
patent: WO 97/02261 (1997-01-01), None
patent: WO 98/21201 (1998-05-01), None
patent: WO 98/28294 (1998-07-01), None
patent: WO 99/38512 (1999-08-01), None
patent: WO 99/38513 (1999-08-01), None
patent: WO 00/78745 (2000-12-01), None
patent: WO 01/02389 (2001-01-01), None
U.S. Pharmacopeia #23, National Formulatory #18 (1995), pp. 1843 and 1844.
Concise Encyclopedia Chemistry, Translated and revised by Mary Eagleson (1994), Walter de Gruyter: New York, pp. 872 and 873.
Rouhi, A. Maureen, “The Right Stuff”, C&E News (Feb. 24, 2003), pp. 32-35.
Curin, A. Sitar, “Study of Crystal Modifications of Lansoprazole using FT-IR . . . ” The Second Central European Symposium on Pharmaceutical Technology (1997), pp. 290 and 291.
Vrecer, F. et al., “Study of Influence of Temperature and Grinding on the . . . ” The Second Central European Symposium on Pharmaceutical Technology (1997), pp. 242 and 243.
Katsuki, H. et al., Determination of R(+)- and S(−)- Lansoprazole Using Chiral Stationary-Phase Liquid . . . , Pharmaceutical Research, vol. 13, No. 4, (1996), pp. 611-615.
Nagaya, H. et al., Effects of the Enantiomers of Lansoprazole (AG-1749) . . . , Biochemical Pharmacology, vol. 42, No. 10 (1991), pp. 1875-1878.
“Experimental Chemistry: Organic Reactions”, JP Document and English Translation, vol. 18, published May 23, 1957.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Process for producing crystal does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Process for producing crystal, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Process for producing crystal will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4118495

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.