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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357747Generated: October 31, 2026

Furosemide → 5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyl chloride

https://huagongshe.com/reaction/2357747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurosemideHCID 3440—
ReactantOxalyl chlorideHCID 65578—
SolventDichloromethaneHCID 6344—
Product5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyl chlorideHCID 86613432—

Reaction Steps

A solution of oxalyl chloride (0.040 mole) in dichloromethane (20 mL) is added dropwise to an ice bath cooled solution of furosemide (5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoic acid), (10) (Aldrich) (0.040 mole) in dichloromethane (50 mL). The reaction is stirred at ambient temperature for 5 hours. The reaction solution is washed with 5% aqueous sodium bicarbonate, with water, and then with a saturated sodium chloride solution. The organic layer is dried over sodium sulfate, filtered and concentrated in vacuo to give 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyl chloride (13). See D. L. Musso, et. al., J. Med. Chem., (2003) 46: 409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763612B2
Source datasetuspto-grants-2010_07
ORD IDord-7097387c96694381a567243c492ee92a
Source noteuspto-grants-2010_07