(19)
(11) EP 1 384 722 A8

(12) CORRECTED EUROPEAN PATENT APPLICATION

(48) Corrigendum issued on:
08.09.2004 Bulletin 2004/37

(43) Date of publication:
28.01.2004 Bulletin 2004/05

(21) Application number: 03020538.9

(22) Date of filing: 19.03.1999
(51) International Patent Classification (IPC)7C07D 413/12, C07D 263/32, C07C 233/47
(84) Designated Contracting States:
AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE
Designated Extension States:
AL LT LV MK RO SI

(30) Priority: 30.03.1998 JP 10409898

(62) Application number of the earlier application in accordance with Art. 76 EPC:
99909293.5 / 0992503

(71) Applicant: Japan Tobacco Inc.
Tokyo 105-8422 (JP)

(72) Inventors:
  • Ando, Koji, 1-1, Murasaki-cho
    Takatsuki-shi Osaka 569-1125 (JP)
  • Suzuki, Masanobu
    Tokyo 184-0004 (JP)

(74) Representative: von Kreisler, Alek, Dipl.-Chem. et al
Patentanwälte, von Kreisler-Selting-Werner, Bahnhofsvorplatz 1 (Deichmannhaus)
50667 Köln
50667 Köln (DE)

 
Remarks:
This application was filed on 17 - 09 - 2003 as a divisional application to the application mentioned under INID code 62.
 


(54) Process for the production of 2-(5-methyl-4-oxazolyl)acetates


(57) The present invention relates to a novel method for producing a compound of the formula [11] wherein R is an optionally substituted aromatic hydrocarbon group, an optionally substituted alicyclic hydrocarbon group, an optionally substituted heterocyclic group or an optionally substituted condensed heterocyclic group, which is useful as a therapeutic agent for diabetes. The method of the present invention is an industrially utilizable method that enables efficient production of the objective compound [11] from β-methyl L-aspartate via an important intermediate compound [6] wherein R is as defined above, at high yield.