Dehydroindapamide
Dehydroindapamide is a structurally modified analog of the parent drug, featuring a chlorosulfonyl group conjugated to a pyridine ring via an oxazole bridge. Its core scaffold incorporates a 1,3-thiazine moiety with a para-chlorophenyl substituent, conferring enhanced lipophilicity. The dehydro prefix denotes an oxidized state relative to the parent compound, characterized by an additional carbonyl functionality at the indane backbone. This compound serves as a critical intermediate in the synthesis of sulfonamide-based diuretics, enabling regioselective functionalization of the aromatic heterocycle during API development.
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Molecular Formula
C16H14ClN3O3S
Molecular Weight
363.8000
CAS Number
63968-75-2
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PubChem CID
45748 ↗
IUPAC Name
4-chloro-N-(2-methylindol-1-yl)-3-sulfamoylbenzamide
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Official Reference Standards
| Std | Catalog # | Quantity | Price |
|---|---|---|---|
| EP | I0150020 ↗ | 15 MG | EUR 90.00 |
| USP | 1338812 ↗ | 50 mg | USD 884.00 |
📝 Synonyms
63968-75-2
Dehydroindapamide
4-chloro-N-(2-methyl-1H-indol-1-yl)-3-sulfamoylbenzamide
BRN 4567208
UNII-AZ0ETT16DT
AZ0ETT16DT
4-Chloro-N-(2-methyl-1-indolyl)-3-sulfamoylbenzamide
Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2-methyl-1H-indol-1-yl)-
4-Chloro-3-sulfamoyl-N-(2-methyl-1H-indol-1-yl)benzamide
BENZAMIDE, 4-CHLORO-N-(2-METHYL-1-INDOLYL)-3-SULFAMOYL-
🔬 Chemical Identifiers
CC1=CC2=CC=CC=C2N1NC(=O)C3=CC(=C(C=C3)Cl)S(=O)(=O)N
InChI=1S/C16H14ClN3O3S/c1-10-8-11-4-2-3-5-14(11)20(10)19-16(21)12-6-7-13(17)15(9-12)24(18,22)23/h2-9H,1H3,(H,19,21)(H2,18,22,23)
LWCDXWWLUHMMJI-UHFFFAOYSA-N
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