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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676909Generated: October 25, 2026

Bumetanide → N,N-diethylaminocarbonylmethyl 3-aminosulfonyl-5-butylamino-4-phenoxybenzoate

https://huagongshe.com/reaction/1676909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBumetanideHCID 2471—
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantChloro-N,N-diethylacetamideHCID 16844—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN,N-diethylaminocarbonylmethyl 3-aminosulfonyl-5-butylamino-4-phenoxybenzoateHCID 1665724163.6%

Reaction Conditions

Temperature95 °C

Reaction Steps

Bumetanide (1.2 g, 3.29 mmol) was dissolved in dimethylformamide (12 mL) and 2-chloro-N,N-diethylacetamide (500 mg, 3.35 mmol) was added followed by triethylamine (0.68 mL) and sodium iodide (500 mg 3.33 mmol). The reaction was heated to 95° C. for 8 hours, at which time TLC and LC/MS indicated the reaction was complete. The reaction was cooled to room temperature brought up in dichloromethane and washed with water, saturated ammonium chloride and reduced to a thick slurry. To the slurry was added water (25 mL), and the resultant solids precipitated from the solution. The product was filtered and dried in a vacuum oven at 50° C. for 12 hours to yield 1.0 g of N,N-diethylaminocarbonylmethyl 3-aminosulfonyl-5-butylamino-4-phenoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008283B2
Source datasetuspto-grants-2011_08
ORD IDord-57c9f7a2ffad4d7c8419fcd840a53bf9
Source noteuspto-grants-2011_08