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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357741Generated: October 30, 2026

Oxalyl chloride → 4-(3-(5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxy)propoxy)(4-oxo)butanoyl chloride

https://huagongshe.com/reaction/2357741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59389123HCID 59389123—
SolventDichloromethaneHCID 6344—
Product4-(3-(5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxy)propoxy)(4-oxo)butanoyl chlorideHCID 86613434—

Reaction Steps

A solution of oxalyl chloride (0.040 mole) in dichloromethane (20 mL) is added dropwise to an ice bath cooled solution of 4-(3-(5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxy)propoxy)(4-oxo)butanoic acid (810) (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 provide 4-(3-(5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoyloxy)propoxy)(4-oxo)butanoyl chloride (813). See eg., 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-a5476f7abb7e4dacb7dda8b94fdb3161
Source noteuspto-grants-2010_07