Synthesis of sulfonylurea derivatives used as oral antidiabetics by the selenium-assisted carbonylation using carbon monoxide with sulfur

Synthetic Communications

Volumn 30, Issue 17, 2000, Pages 3081-3089

  Mizuno, Takumi ^a   Kino, Takanobu ^a   Ito, Takatoshi ^a   Miyata, Toshiyuki ^a  

^a OSAKA MUNICIPAL TECHNICAL RESEARCH INSTITUTE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; BENZENESULFONAMIDE DERIVATIVE; CARBON MONOXIDE; CHLORPROPAMIDE; METHYL IODIDE; ORAL ANTIDIABETIC AGENT; SULFONYLUREA DERIVATIVE; SULFUR; THIOCARBAMIC ACID DERIVATIVE; TOLBUTAMIDE;

ARTICLE; CATALYSIS; CHEMICAL MODIFICATION; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS; STOICHIOMETRY;

EID: 0033866025     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397910008086914     Document Type: Article

References (6)

1. Budavari, S. (ed.) "THE MERCK INDEX 11 th" MERCK & CO., INC, Rahway, N. J., 1989, pp 1497.
2. Budavari, S. (ed.) "THE MERCK INDEX 11 th" MERCK & CO., INC, Rahway, N. J., 1989, pp 338.
3. Sonoda, N., Mizuno, T., Murakami, S., Kondo, K., Ogawa, A., Ryu, I., and Kambe, N. Angew. Chem. Int. Ed. Engl., 1989, 28, 452.
4. Mizuno, T., Nishiguchi, I., and Sonoda, N. Tetrahedron, 1994, 50, 5669.
5. 3,4 6. Dibutylurea was also formed (0.14g, 8%).
6. It was identified by the comparison of spectrum of library search (MS-WILEY D6).