Hydroflumethiazide

Chemical compound
  • C03AA02 (WHO)
Identifiers
  • 1,1-Dioxo-6-(trifluoromethyl)-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide
CAS Number
  • 135-09-1 checkY
PubChem CID
  • 3647
IUPHAR/BPS
  • 7197
DrugBank
  • DB00774 checkY
ChemSpider
  • 3521 checkY
UNII
  • 501CFL162R
KEGG
  • D00654 checkY
ChEMBL
  • ChEMBL1763 checkY
CompTox Dashboard (EPA)
  • DTXSID3023132 Edit this at Wikidata
ECHA InfoCard100.004.704 Edit this at WikidataChemical and physical dataFormulaC8H8F3N3O4S2Molar mass331.28 g·mol−13D model (JSmol)
  • Interactive image
  • FC(F)(F)c2c(cc1c(NCNS1(=O)=O)c2)S(=O)(=O)N
InChI
  • InChI=1S/C8H8F3N3O4S2/c9-8(10,11)4-1-5-7(2-6(4)19(12,15)16)20(17,18)14-3-13-5/h1-2,13-14H,3H2,(H2,12,15,16) checkY
  • Key:DMDGGSIALPNSEE-UHFFFAOYSA-N checkY
  (verify)

Hydroflumethiazide (or Saluron) is a diuretic.

Synthesis

Hydroflumethiazide synthesis:[1][2][3] Numerous patents, e.g., Lund et al., U.S. patent 3,254,076 (1966 to Lövens Kemiske Fabrik).

See also

  • Bendroflumethiazide

References

  1. ^ Holdrege CT, Babel RB, Cheney LC (1959). "Synthesis of Trifluoromethylated Compounds Possessing Diuretic Activity1". Journal of the American Chemical Society. 81 (18): 4807–4810. doi:10.1021/ja01527a015.
  2. ^ Close WJ, Swett LR, Brady LE, Short JH, Vernsten M (1960). "Synthesis of Potential Diuretic Agents. I. Derivatives of 7-Sulfamyl-3,4-dihydro-1,2,4-benzothiadiazine 1,1-Dioxide". Journal of the American Chemical Society. 82 (5): 1132–1135. doi:10.1021/ja01490a028.
  3. ^ Novello FC, Bell SC, Abrams EL, Ziegler C, Sprague JM (1960). "Diuretics: 1,2,4-Benzothiadiazine-1,1-dioxides". The Journal of Organic Chemistry. 25 (6): 970–981. doi:10.1021/jo01076a028.
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Sulfonamides
(and etacrynic acid)
CA inhibitors (at PT)
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Calcium-sparing)
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