Preparation of N-[(imidazopyridinylamino)methylphenyl]carbamates and analogs as gastric acid secretion inhibitors.

  • Riedel R
  • Postius S
  • Simon W
  • et al.
N/ACitations
Citations of this article
2Readers
Mendeley users who have this article in their library.

Abstract

Title compds. (I; R = Me or CH2OH; R1 = alkyl; R2,R4 = H, halo, alkyl, alkoxy, CF3; R3 = alkoxy; R5 = H, halo, alkyl, alkoxy; Z = O or NH) were prepd. Thus, 8-amino-2-methylimidazo[1,2-a]pyridine-3-carboxaldehyde was N-alkylated by 3,2-Cl(ClH2C)C6H3NHCO2Me and the product reduced to give I (R = CH2OH, R1 = Me, R2 = Cl, R3 = OMe, R4 = R5 = H, Z = NH) which gave 97% inhibition of pentagastrin-induced gastric acid secretion in rats at 6μmol/kg i.v. [on SciFinder(R)]

Cite

CITATION STYLE

APA

Riedel, R., Postius, S., Simon, W.-A., Rainer, G., Senn-Bilfinger, J., & Grundler, Gerhard. (1996). Preparation of N-[(imidazopyridinylamino)methylphenyl]carbamates and analogs as gastric acid secretion inhibitors. PCT Int. Appl. Byk Gulden Lomberg Chemische Fabrik Gmbh, Germany .

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free