Tripamide

Tripamide

Clinical data
AHFS/Drugs.com	International Drug Names
Routes of administration	Oral
ATC code	none
Legal status
Legal status	In general: ℞ (Prescription only)
Identifiers
IUPAC name 3-(aminosulfonyl)-4-chloro-N-[(3aR,4S,7R,7aS)-octahydro-2H-4,7-methanoisoindol-2-yl]benzamide
CAS Number	73803-48-2
PubChem CID	636401
DrugBank	DB15959 Y
ChemSpider	4445396
UNII	G36A0E9CVT
ChEMBL	ChEMBL2104484
CompTox Dashboard (EPA)	DTXSID2057817
Chemical and physical data
Formula	C16H20ClN3O3S
Molar mass	369.86 g·mol−1
3D model (JSmol)	Interactive image
SMILES C1C[C@@H]2C[C@H]1[C@@H]3[C@H]2CN(C3)NC(=O)C4=CC(=C(C=C4)Cl)S(=O)(=O)N
InChI InChI=1S/C16H20ClN3O3S/c17-14-4-3-11(6-15(14)24(18,22)23)16(21)19-20-7-12-9-1-2-10(5-9)13(12)8-20/h3-4,6,9-10,12-13H,1-2,5,7-8H2,(H,19,21)(H2,18,22,23)/t9-,10+,12-,13+ Key:UHLOVGKIEARANS-NIFPGPBJSA-N
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Tripamide (INN) is a diuretic.

Diels-Alder reaction between maleimide and cyclopentadiene gives a compound that is called noreximide [6319-06-8]. This compound is of utility not merely in the production of tripamide, but also in the synthesis of taglutimide, lurasidone, tandospirone, perospirone (close) and lastly a pesticide that is called MGK 264.

Tecovirimat has a structure that is related to tripamide but with some important differences.