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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566218Generated: October 27, 2026

Hydrochloric Acid → 5-Chloro-3-(5-bromo-2-furanoyl)-2-oxindole-1-carboxamide

https://huagongshe.com/reaction/566218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
Reactant5-Bromofuran-2-carbonyl chlorideHCID 2757011—
Reactant5-Chloro-2-oxo-2,3-dihydro-1H-indole-1-carboxamideHCID 9859159—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventThionyl ChlorideHCID 24386—
Product5-Chloro-3-(5-bromo-2-furanoyl)-2-oxindole-1-carboxamideHCID 86745043—

Reaction Steps

Using the procedure of Example 32, 1.91 g (10.0 mmoless) of commercially available 5-bromo-2-furancarboxylic acid was dissolved in 10 ml of thionyl chloride and heated to reflux under nitrogen for 1 hour and the acid chloride product was recovered. A 40 ml N,N-dimethylformamide solution of 1.75 g (8.3 mmoles) of 5-chloro-2-oxindole-1-carboxamide and 3.05 g (25 mmoles) of 4-(N,N-dimethylamino)pyridine was reacted with 2.09 g (10 mmoles) of 5-bromo-2-furan carbonyl chloride in 10 ml of N,N-dimethylformamide. After a reaction time of about 45 minutes, the mixture was acidified by pouring into 250 ml of 1N HCl. The product was recrystallized from acetic acid, washed with acetic acid, then hexane and dried overnight in vacuo at room temperature. The resulting product then was dried over refluxing isopropanol under high vacuum to yield 1.37 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174883B1
Source datasetuspto-grants-2001_01
ORD IDord-486ee0ba054148669d0eefd803db226c
Source noteuspto-grants-2001_01